Radionuclide(Redirected from Radioactive material)
A radionuclide (radioactive nuclide, radioisotope or radioactive isotope) is an atom that has excess nuclear energy, making it unstable. This excess energy can be used in one of three ways: emitted from the nucleus as gamma radiation; transferred to one of its electrons to release it as a conversion electron; or used to create and emit a new particle (alpha particle or beta particle) from the nucleus. During those processes, the radionuclide is said to undergo radioactive decay. These emissions are considered ionizing radiation because they are powerful enough to liberate an electron from another atom. The radioactive decay can produce a stable nuclide or will sometimes produce a new unstable radionuclide which may undergo further decay. Radioactive decay is a random process at the level of single atoms: it is impossible to predict when one particular atom will decay. However, for a collection of atoms of a single element the decay rate, and thus the half-life (t1/2) for that collection can be calculated from their measured decay constants. The range of the half-lives of radioactive atoms have no known limits and span a time range of over 55 orders of magnitude.
Radionuclides occur naturally or are artificially produced in nuclear reactors, cyclotrons, particle accelerators or radionuclide generators. There are about 730 radionuclides with half-lives longer than 60 minutes (see list of nuclides). Thirty-two of those are primordial radionuclides that were created before the earth was formed. At least another 60 radionuclides are detectable in nature, either as daughters of primordial radionuclides or as radionuclides produced through natural production on Earth by cosmic radiation. More than 2400 radionuclides have half-lives less than 60 minutes. Most of those are only produced artificially, and have very short half-lives. For comparison, there are about 253 stable nuclides. (In theory, only 146 of them are stable, and the other 107 are believed to decay (alpha decay or beta decay or double beta decay or electron capture or double electron capture))
All chemical elements can exist as radionuclides. Even the lightest element, hydrogen, has a well-known radionuclide, tritium. Elements heavier than lead, and the elements technetium and promethium, exist only as radionuclides. (In theory, elements heavier than dysprosium exist only as radionuclides, but the half-life for some such elements (e.g. gold and platinum) are too long to found)
Unplanned exposure to radionuclides generally has a harmful effect on living organisms including humans, although low levels of exposure occur naturally without harm. The degree of harm will depend on the nature and extent of the radiation produced, the amount and nature of exposure (close contact, inhalation or ingestion), and the biochemical properties of the element; with increased risk of cancer the most usual consequence. However, radionuclides with suitable properties are used in nuclear medicine for both diagnosis and treatment. An imaging tracer made with radionuclides is called a radioactive tracer. A pharmaceutical drug made with radionuclides is called a radiopharmaceutical.
On Earth, naturally occurring radionuclides fall into three categories: primordial radionuclides, secondary radionuclides, and cosmogenic radionuclides.
- Radionuclides are produced in stellar nucleosynthesis and supernova explosions along with stable nuclides. Most decay quickly but can still be observed astronomically and can play a part in understanding astronomic processes. Primordial radionuclides, such as uranium and thorium, exist in the present time because their half-lives are so long (>100 million years) that they have 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 notably bismuth-209: detection of this decay meant that bismuth was no longer considered stable. It is possible decay may be observed in other nuclides adding to this list of primordial radionuclides.
- Secondary radionuclides are radiogenic isotopes derived from the decay of primordial radionuclides. They have shorter half-lives than primordial radionuclides. They arise in the decay chain of the primordial isotopes thorium-232, uranium-238 and uranium-235. Examples include the natural isotopes of polonium and radium.
- Cosmogenic isotopes, such as carbon-14, are present because they are continually being formed in the atmosphere due to cosmic rays.
Many of these radionuclides exist only in trace amounts in nature, including all cosmogenic nuclides. Secondary radionuclides will occur in proportion to their half-lives, so short-lived ones will be very rare. Thus polonium can be found in uranium ores at about 0.1 mg per metric ton (1 part in 1010). Further radionunclides may occur in nature in virtually undetectable amounts as a result of rare events such as spontaneous fission or uncommon cosmic ray interactions.
Radionuclides are produced as an unavoidable result of nuclear fission and thermonuclear explosions. The process of nuclear fission creates a wide range of fission products, most of which are radionuclides. Further radionuclides can be created from irradiation of the nuclear fuel (creating a range of actinides) and of the surrounding structures, yielding activation products. This complex mixture of radionuclides with different chemistries and radioactivity makes handling nuclear waste and dealing with nuclear fallout particularly problematic.
Synthetic radionuclides are deliberately synthesised using nuclear reactors, particle accelerators or radionuclide generators:
- As well as being extracted from nuclear waste, radioisotopes can be produced deliberately with nuclear reactors, exploiting the high flux of neutrons present. These neutrons activate elements placed within the reactor. A typical product from a nuclear reactor is iridium-192. The elements that have a large propensity to take up the neutrons in the reactor are said to have a high neutron cross-section.
- Particle accelerators such as cyclotrons accelerate particles to bombard a target to produce radionuclides. Cyclotrons accelerate protons at a target to produce positron-emitting radionuclides, e.g. fluorine-18.
- Radionuclide generators contain a parent radionuclide that decays to produce a radioactive daughter. The parent is usually produced in a nuclear reactor. A typical example is the technetium-99m generator used in nuclear medicine. The parent produced in the reactor is molybdenum-99.
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).
- In biology, radionuclides of carbon can serve as radioactive tracers because they are chemically very similar to the nonradioactive nuclides, so most chemical, biological, and ecological processes treat them in a nearly identical way. One can then examine the result with a radiation detector, such as a Geiger counter, to determine where the provided atoms were incorporated. For example, one might culture plants in an environment in which the carbon dioxide contained radioactive carbon; then the parts of the plant that incorporate atmospheric carbon would be radioactive. Radionuclides can be used to monitor processes such as DNA replication or amino acid transport.
- In nuclear medicine, radioisotopes are used for diagnosis, treatment, and research. Radioactive chemical tracers emitting gamma rays or positrons can provide diagnostic information about internal anatomy and the functioning of specific organs, including the human brain. This is used in some forms of tomography: single-photon emission computed tomography and positron emission tomography (PET) scanning and Cherenkov luminescence imaging. Radioisotopes are also a method of treatment in hemopoietic forms of tumors; the success for treatment of solid tumors has been limited. More powerful gamma sources sterilise syringes and other medical equipment.
- In food preservation, radiation is used to stop the sprouting of root crops after harvesting, to kill parasites and pests, and to control the ripening of stored fruit and vegetables.
- In industry, and in mining, radionuclides are used to examine welds, to detect leaks, to study the rate of wear, erosion and corrosion of metals, and for on-stream analysis of a wide range of minerals and fuels.
- In spacecraft and elsewhere, radionuclides are used to provide power and heat, notably through radioisotope thermoelectric generators (RTGs).
- In astronomy and cosmology radionuclides play a role in understanding stellar and planetary process.
- In particle physics, radionuclides help discover new physics (physics beyond the Standard Model) by measuring the energy and momentum of their beta decay products.
- In ecology, radionuclides are used to trace and analyze pollutants, to study the movement of surface water, and to measure water runoffs from rain and snow, as well as the flow rates of streams and rivers.
- In geology, archaeology, and paleontology, natural radionuclides are used to measure ages of rocks, minerals, and fossil materials.
The following table lists properties of selected radionuclides illustrating the range of properties and uses.
|Mode of formation||Comments|
|Tritium (3H)||1||2||12.3 y||β−||19||Cosmogenic||lightest radionuclide, used in artificial nuclear fusion, also used for radioluminescence and as oceanic transient tracer. Synthesized from neutron bombardment of lithium-6 or deuterium|
|Beryllium-10||4||6||1,387,000 y||β−||556||Cosmogenic||used to examine soil erosion, soil formation from regolith, and the age of ice cores|
|Carbon-14||6||8||5,700 y||β−||156||Cosmogenic||used for radiocarbon dating|
|Fluorine-18||9||9||110 min||β+, EC||633/1655||Cosmogenic||positron source, synthesised for use as a medical radiotracer in PET scans.|
|Aluminium-26||13||13||717,000 y||β+, EC||4004||Cosmogenic||exposure dating of rocks, sediment|
|Chlorine-36||17||19||301,000 y||β−, EC||709||Cosmogenic||exposure dating of rocks, groundwater tracer|
|Potassium-40||19||21||1.24×109 y||β−, EC||1330 /1505||Primordial||used for potassium-argon dating, source of atmospheric argon, source of radiogenic heat, largest source of natural radioactivity|
|Calcium-41||20||21||102,000 y||EC||Cosmogenic||exposure dating of carbonate rocks|
|Cobalt-60||27||33||5.3 y||β−||2824||Synthetic||produces high energy gamma rays, used for radiotherapy, equipment sterilisation, food irradiation|
|Strontium-90||38||52||28.8 y||β−||546||Fission product||medium-lived fission product; probably most dangerous component of nuclear fallout|
|Technetium-99||43||56||210,000 y||β−||294||Fission product||commonest isotope of the lightest unstable element, most significant of long-lived fission products|
|Technetium-99m||43||56||6 hr||γ,IC||141||Synthetic||most commonly used medical radioisotope, used as a radioactive tracer|
|Iodine-129||53||76||15,700,000 y||β−||194||Cosmogenic||longest lived fission product; groundwater tracer|
|Iodine-131||53||78||8 d||β−||971||Fission product||most significant short term health hazard from nuclear fission, used in nuclear medicine, industrial tracer|
|Xenon-135||54||81||9.1 h||β−||1160||Fission Product||strongest known "nuclear poison" (neutron-absorber), with a major effect on nuclear reactor operation.|
|Caesium-137||55||82||30.2 y||β−||1176||Fission Product||other major medium-lived fission product of concern|
|Gadolinium-153||64||89||240 d||EC||Synthetic||Calibrating nuclear equipment, bone density screening|
|Bismuth-209||83||126||1.9×1019y||α||3137||Primordial||long considered stable, decay only detected in 2003|
|Polonium-210||84||126||138 d||α||5307||Decay Product||Highly toxic, used in poisoning of Alexander Litvinenko|
|Radon-222||86||136||3.8d||α||5590||Decay Product||gas, responsible for the majority of public exposure to ionizing radiation, second most frequent cause of lung cancer|
|Thorium-232||90||142||1.4×1010 y||α||4083||Primordial||basis of thorium fuel cycle|
|Uranium-235||92||143||7×108y||α||4679||Primordial||fissile, main nuclear fuel|
|Uranium-238||92||146||4.5×109 y||α||4267||Primordial||Main Uranium isotope|
|Plutonium-238||94||144||87.7 y||α||5593||Synthetic||used in radioisotope thermoelectric generators (RTGs) and radioisotope heater units as an energy source for spacecraft|
|Plutonium-239||94||145||24110 y||α||5245||Synthetic||used for most modern nuclear weapons|
|Americium-241||95||146||432 y||α||5486||Synthetic||used in household smoke detectors as an ionising agent|
|Californium-252||98||154||2.64 y||α/SF||6217||Synthetic||undergoes spontaneous fission (3% of decays), making it a powerful neutron source, used as a reactor initiator and for detection devices|
Key: Z = no of protons; N = no of Neutrons; DM = Decay Mode; DE = Decay Energy; EC = Electron Capture
Household smoke detectorsEdit
Radionuclides are present in many homes as they are used inside the most common household smoke detectors. The radionuclide used is americium-241, which is created by bombarding plutonium with neutrons in a nuclear reactor. It decays by emitting alpha particles and gamma radiation to become neptunium-237. Smoke detectors use a very small quantity of 241Am (about 0.29 micrograms per smoke detector) in the form of americium dioxide. 241Am is used as it emits alpha particles which ionise the air in the detector's ionization chamber. A small electric voltage is applied to the ionised 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.
Impacts on organismsEdit
Radionuclides that find their way into the environment may cause harmful effects as radioactive contamination. They can also cause damage if they are excessively used during treatment or in other ways exposed to living beings, by radiation 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, to radiation burns and acute 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."
Summary table for classes of nuclides, "stable" and radioactiveEdit
Following is a summary table for the total list of nuclides with half-lives greater than one hour. Ninety of these 989 nuclides are theoretically stable, except to proton-decay (which has never been observed). About 253 nuclides have never been observed to decay, and are classically considered stable.
The remaining 662 radionuclides have half-lives longer than 1 hour, and are well-characterized (see list of nuclides for a complete tabulation). They include 28 nuclides with measured half-lives longer than the estimated age of the universe (13.8 billion years), and another 4 nuclides with half-lives long enough (> 100 million years) that they are radioactive primordial nuclides, and may be detected on Earth, having survived from their presence in interstellar dust since before the formation of the solar 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 artificial nuclear transmutation.
Numbers are not exact, and may change slightly in the future, as "stable nuclides" are observed to be radioactive with very long half-lives.
|Stability class||Number of nuclides||Running total||Notes on running total|
|Theoretically stable to all but proton decay||90||90||Includes first 40 elements. Proton decay yet to be observed.|
|Theoretically stable to alpha decay, beta decay, isomeric transition, and double beta decay but not spontaneous fission, which is possible for "stable" nuclides ≥ niobium-93||56||146||All nuclides that are possible 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.||107||253||Total of classically stable nuclides.|
|Radioactive primordial nuclides.||33||286||Total primordial elements include uranium, thorium, bismuth, rubidium-87, potassium-40, tellurium-128 plus all stable nuclides.|
|Radioactive nonprimordial, but naturally occurring on Earth.||61||347||Carbon-14 (and other isotopes generated by cosmic rays) and daughters of radioactive primordial elements, such as radium, polonium, etc. 41 of these have a half life of greater than one hour.|
|Radioactive synthetic half-life ≥ 1.0 hour). Includes most useful radiotracers.||662||989||These 989 nuclides are listed in the article List of nuclides.|
|Radioactive synthetic (half-life < 1.0 hour).||>2400||>3300||Includes all well-characterized synthetic nuclides.|
List of commercially available radionuclidesEdit
This list covers common isotopes, most of which are available in very small quantities to the general public in most countries. Others that are not publicly accessible are traded commercially in industrial, medical, and scientific fields and are subject to government regulation.
Gamma emission onlyEdit
|Barium-133||9694 TBq/kg (262 Ci/g)||10.7 years||81.0, 356.0|
|Cadmium-109||96200 TBq/kg (2600 Ci/g)||453 days||88.0|
|Cobalt-57||312280 TBq/kg (8440 Ci/g)||270 days||122.1|
|Cobalt-60||40700 TBq/kg (1100 Ci/g)||5.27 years||1173.2, 1332.5|
|Europium-152||6660 TBq/kg (180 Ci/g)||13.5 years||121.8, 344.3, 1408.0|
|Manganese-54||287120 TBq/kg (7760 Ci/g)||312 days||834.8|
|Sodium-22||237540 Tbq/kg (6240 Ci/g)||2.6 years||511.0, 1274.5|
|Zinc-65||304510 TBq/kg (8230 Ci/g)||244 days||511.0, 1115.5|
|Technetium-99m||×107 TBq/kg (5.27 × 105 Ci/g) 1.95||6 hours||140|
Beta emission onlyEdit
|Strontium-90||5180 TBq/kg (140 Ci/g)||28.5 years||546.0|
|Thallium-204||17057 TBq/kg (461 Ci/g)||3.78 years||763.4|
|Carbon-14||166.5 TBq/kg (4.5 Ci/g)||5730 years||49.5 (average)|
|Tritium (Hydrogen-3)||357050 TBq/kg (9650 Ci/g)||12.32 years||5.7 (average)|
Alpha emission onlyEdit
|Polonium-210||166500 TBq/kg (4500 Ci/g)||138.376 days||5304.5|
|Uranium-238||12580 KBq/kg (0.00000034 Ci/g)||4.468 billion years||4267|
Multiple radiation emittersEdit
|Isotope||Activity||Half-life||Radiation types||Energies (keV)|
|Caesium-137||3256 TBq/kg (88 Ci/g)||30.1 years||Gamma & beta||G: 32, 661.6 B: 511.6, 1173.2|
|Americium-241||129.5 TBq/kg (3.5 Ci/g)||432.2 years||Gamma & alpha||G: 59.5, 26.3, 13.9 A: 5485, 5443|
- R.H. Petrucci, W.S. Harwood and F.G. Herring, General Chemistry (8th ed., Prentice-Hall 2002), p.1025–26
- "Decay and Half Life". Retrieved 2009-12-14.
- Stabin, Michael G. (2007). "3". Radiation Protection and Dosimetry: An Introduction to Health Physics (Submitted manuscript). Springer. doi:10.1007/978-0-387-49983-3. ISBN 978-0387499826.
- Best, Lara; Rodrigues, George; Velker, Vikram (2013). "1.3". Radiation Oncology Primer and Review. Demos Medical Publishing. ISBN 978-1620700044.
- Loveland, W.; Morrissey, D.; Seaborg, G.T. (2006). Modern Nuclear Chemistry. Modern Nuclear Chemistry. Wiley-Interscience. p. 57. Bibcode:2005mnc..book.....L. ISBN 978-0-471-11532-8.
- Eisenbud, Merril; Gesell, Thomas F (1997-02-25). Environmental Radioactivity: From Natural, Industrial, and Military Sources. p. 134. ISBN 9780122351549.
- Bagnall, K. W. (1962). "The Chemistry of Polonium". Advances in Inorganic Chemistry and Radiochemistry 4. New York: Academic Press. pp. 197–226. doi:10.1016/S0065-2792(08)60268-X. ISBN 0-12-023604-4. Retrieved June 14, 2012., p. 746
- Bagnall, K. W. (1962). "The Chemistry of Polonium". Advances in Inorganic Chemistry and Radiochemistry 4. New York: Academic Press., p. 198
- Ingvar, David H.; 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.
- Ingvar, David H.; Franzén, Göran (1974). "Distribution of cerebral activity in chronic schizophrenia". The Lancet. 304 (7895): 1484–1486. doi:10.1016/s0140-6736(74)90221-9.
- Lassen, Niels A.; Ingvar, David H.; Skinhøj, Erik (October 1978). "Brain Function and Blood Flow" (PDF). Scientific American. 239 (4): 62–71. Bibcode:1978SciAm.239d..62L. doi:10.1038/scientificamerican1078-62.
- 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.
- "Smoke Detectors and Americium". world-nuclear.org. Archived from the original on 2010-11-12.
- Office of Radiation Protection – Am 241 Fact Sheet – Washington State Department of Health Archived 2011-03-18 at the Wayback Machine.
- "Ionizing radiation, health effects and protective measures". World Health Organization. November 2012. Retrieved January 27, 2014.
- "Cosmic Detectives". The European Space Agency (ESA). 2013-04-02. Retrieved 2013-04-15.
- Table data is derived by counting members of the list; see WP:CALC. References for the list data itself are given below in the reference section in list of nuclides
- Carlsson, J.; Forssell Aronsson, E; Hietala, SO; Stigbrand, T; Tennvall, J; et al. (2003). "Tumour therapy with radionuclides: assessment of progress and problems". Radiotherapy and Oncology. 66 (2): 107–117. doi:10.1016/S0167-8140(02)00374-2. PMID 12648782.
- "Radioisotopes in Industry". World Nuclear Association.
- Martin, James (2006). Physics for Radiation Protection: A Handbook. p. 130. ISBN 978-3527406111.
|Wikimedia Commons has media related to |
- EPA – Radionuclides – EPA's Radiation Protection Program: Information.
- FDA – Radionuclides – FDA's Radiation Protection Program: Information.
- Interactive Chart of Nuclides – A chart of all nuclides
- National Isotope Development Center – U.S. Government source of radionuclides – production, research, development, distribution, and information
- The Live Chart of Nuclides – IAEA