Californium: Difference between revisions

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{{infobox californium}}
{{infobox californium}}
'''Californium''' is a [[synthetic element|synthetic chemical element]]; it has [[Chemical symbol|symbol]] '''Cf''' and [[atomic number]] 98. It was first synthesized in 1950 at [[Lawrence Berkeley National Laboratory]] (then the University of California Radiation Laboratory) by bombarding [[curium]] with [[alpha particle]]s ([[helium-4]] ions). It is an [[actinide]] element, the sixth [[transuranium element]] to be [[synthetic element|synthesized]], and has the second-highest atomic mass of all elements that have been produced in amounts large enough to see with the [[naked eye]] (after [[einsteinium]]). It was named after the university and the [[U.S. state]] of [[California]].
'''Californium''' is a [[synthetic element|synthetic chemical element]]; it has [[Chemical symbol|symbol]] '''Cf''' and [[atomic number]] 98. It was first synthesized in 1950 at [[Lawrence Berkeley National Laboratory]] (then the University of California Radiation Laboratory) by bombarding [[curium]] with [[alpha particle]]s ([[helium-4]] ions). It is an [[actinide]] element, the sixth [[transuranium element]] to be [[synthetic element|synthesized]], and has the second-highest atomic mass of all elements that have been produced in amounts large enough to see with the [[naked eye]] (after [[einsteinium]]). It was named after the [[University of California, Berkeley|university]] and the [[U.S. state]] of [[California]].


Two [[crystal structure|crystalline forms]] exist at normal pressure: one above and one below {{convert|900|C|-1}}. A third form exists at high pressure. Californium slowly tarnishes in air at room temperature. [[Californium compounds]] are dominated by the +3 [[oxidation state]]. The most stable of californium's twenty known [[isotope]]s is californium-251, with a [[half-life]] of 898 years. This short half-life means the element is not found in significant quantities in the Earth's crust.{{efn|name=age of earth}} {{sup|252}}Cf, with a half-life of about 2.645 years, is the most common isotope used and is produced at [[Oak Ridge National Laboratory]] (ORNL) in the United States and [[Research Institute of Atomic Reactors]] in Russia.
Two [[crystal structure|crystalline forms]] exist at normal pressure: one above and one below {{convert|900|C|-1}}. A third form exists at high pressure. Californium slowly tarnishes in air at room temperature. [[Californium compounds]] are dominated by the +3 [[oxidation state]]. The most stable of californium's twenty known [[isotope]]s is californium-251, with a [[half-life]] of 898 years. This short half-life means the element is not found in significant quantities in the Earth's crust.{{efn|name=age of earth}} {{sup|252}}Cf, with a half-life of about 2.645 years, is the most common isotope used and is produced at [[Oak Ridge National Laboratory]] (ORNL) in the United States and [[Research Institute of Atomic Reactors]] in Russia.
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=== Isotopes ===
=== Isotopes ===
{{main|Isotopes of californium}}
{{main|Isotopes of californium}}
Twenty [[isotope]]s of californium are known ([[mass number]] ranging from 237 to 256<ref name="NNDC2008" />); the most stable are {{sup|251}}Cf with [[half-life]] 898 years, {{sup|249}}Cf with half-life 351 years, {{sup|250}}Cf at 13.08 years, and {{sup|252}}Cf at 2.645 years.<ref name="NNDC2008" /> All other isotopes have half-life shorter than a year, and most of these have half-lives less than 20 minutes.<ref name="NNDC2008" />
:''All nuclear data not otherwise stated is from the standard source:<ref>{{NUBASE2020}}</ref>''
Twenty [[isotope]]s of californium are known with [[mass number]] ranging from 237 to 256; the most stable are {{sup|251}}Cf with [[half-life]] 898 years, {{sup|249}}Cf with half-life 351 years, {{sup|250}}Cf at 13.08 years, and {{sup|252}}Cf at 2.645 years. All other isotopes have half-life shorter than a year, and most of these have half-lives less than 20 minutes.


{{sup|249}}Cf is formed by [[beta decay]] of berkelium-249, and most other californium isotopes are made by subjecting berkelium to intense neutron radiation in a [[nuclear reactor]].{{sfn|CRC|2006|p=4.8}} Though californium-251 has the longest half-life, its production yield is only 10% due to its tendency to collect neutrons (high [[neutron capture]]) and its tendency to interact with other particles (high [[neutron cross section]]).{{sfn|Haire|2006|p=1504}}
{{sup|249}}Cf is formed by [[beta decay]] of berkelium-249, and heavier californium isotopes are made by subjecting berkelium to intense neutron radiation in a [[nuclear reactor]]. Though californium-251 has the longest half-life, its production yield is relatively low due to its rapid depletion by reaction with another neutron (high [[neutron cross section]]).{{sfn|Haire|2006|p=1504}}


{{sup|252}}Cf is a very strong [[neutron]] emitter, which makes it extremely [[radioactive]] and harmful.<ref>{{cite journal|author = Hicks, D. A. |title = Multiplicity of Neutrons from the Spontaneous Fission of Californium-252|journal = Physical Review|date = 1955|volume = 97|issue = 2|pages = 564–565|doi = 10.1103/PhysRev.97.564|last2 = Ise|first2 = John|last3 = Pyle|first3 = Robert V.|bibcode = 1955PhRv...97..564H |url = http://www.escholarship.org/uc/item/6031k6m2}}</ref><ref>{{cite journal|author = Hicks, D. A. |title = Spontaneous-Fission Neutrons of Californium-252 and Curium-244|journal = Physical Review |date = 1955|volume = 98|issue = 5|pages = 1521–1523|doi = 10.1103/PhysRev.98.1521|last2 = Ise|first2 = John|last3 = Pyle|first3 = Robert V.|bibcode = 1955PhRv...98.1521H }}</ref><ref>{{cite journal|author =Hjalmar, E.|author2 =Slätis, H.|author3 =Thompson, S.G. |title = Energy Spectrum of Neutrons from Spontaneous Fission of Californium-252| journal = Physical Review| date = 1955| volume = 100|issue =5|pages = 1542–1543| doi = 10.1103/PhysRev.100.1542|bibcode = 1955PhRv..100.1542H }}</ref> {{sup|252}}Cf, 96.9% of the time, [[alpha decay]]s to [[curium]]-248; the other 3.1% of decays are [[spontaneous fission]].<ref name="NNDC2008" /> One [[microgram]] (μg) of {{sup|252}}Cf emits 2.3&nbsp;million neutrons per second, an average of 3.7 neutrons per spontaneous fission.<ref name="osti">{{cite journal|author = Martin, R. C.|author2 = Knauer, J. B.|author3 = Balo, P. A.| title = Production, Distribution, and Applications of Californium-252 Neutron Sources| date = 1999|url = http://www.osti.gov/bridge/purl.cover.jsp?purl=/15053-AE6cnN/native/ |doi = 10.1016/S0969-8043(00)00214-1|journal = Applied Radiation and Isotopes |volume = 53|issue = 4–5|pages = 785–92|pmid = 11003521 }}</ref> Most other isotopes of californium, alpha decay to curium ([[atomic number]] 96).<ref name="NNDC2008" />
{{sup|252}}Cf is a very strong [[neutron]] emitter, which makes it an extremely hazardous [[radioactive]] isotope.<ref>{{cite journal|author = Hicks, D. A. |title = Multiplicity of Neutrons from the Spontaneous Fission of Californium-252|journal = Physical Review|date = 1955|volume = 97|issue = 2|pages = 564–565|doi = 10.1103/PhysRev.97.564|last2 = Ise|first2 = John|last3 = Pyle|first3 = Robert V.|bibcode = 1955PhRv...97..564H |url = http://www.escholarship.org/uc/item/6031k6m2}}</ref><ref>{{cite journal|author = Hicks, D. A. |title = Spontaneous-Fission Neutrons of Californium-252 and Curium-244|journal = Physical Review |date = 1955|volume = 98|issue = 5|pages = 1521–1523|doi = 10.1103/PhysRev.98.1521|last2 = Ise|first2 = John|last3 = Pyle|first3 = Robert V.|bibcode = 1955PhRv...98.1521H }}</ref><ref>{{cite journal|author =Hjalmar, E.|author2 =Slätis, H.|author3 =Thompson, S.G. |title = Energy Spectrum of Neutrons from Spontaneous Fission of Californium-252| journal = Physical Review| date = 1955| volume = 100|issue =5|pages = 1542–1543| doi = 10.1103/PhysRev.100.1542|bibcode = 1955PhRv..100.1542H }}</ref> {{sup|252}}Cf, 96.9% of the time, [[alpha decay]]s to [[curium]]-248; the other 3.1% of decays are [[spontaneous fission]]. One [[microgram]] of {{sup|252}}Cf emits 2.3&nbsp;million neutrons per second (about 3.7 neutrons per fission).<ref name="osti">{{cite journal|author = Martin, R. C.|author2 = Knauer, J. B.|author3 = Balo, P. A.| title = Production, Distribution, and Applications of Californium-252 Neutron Sources| date = 1999|url = http://www.osti.gov/bridge/purl.cover.jsp?purl=/15053-AE6cnN/native/ |doi = 10.1016/S0969-8043(00)00214-1|journal = Applied Radiation and Isotopes |volume = 53|issue = 4–5|pages = 785–92|pmid = 11003521 | osti=15053 }}</ref> The other main isotopes of californium (248-251) also alpha decay to those of [[curium]], with a much smaller fraction of fission.


== History ==
== History ==
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The discoverers named the new element after the university and the state. This was a break from the convention used for elements 95 to 97, which drew inspiration from how the elements directly above them in the periodic table were named.{{sfn|Weeks|Leichester|1968|p=849}}{{efn|[[Europium]], in the sixth period directly above element 95, was named for the continent it was discovered on, so element 95 was named [[americium]]. Element 96 was named [[curium]] for [[Marie Curie]] and [[Pierre Curie]] as an analog to the naming of [[gadolinium]], which was named for the scientist and engineer [[Johan Gadolin]]. [[Terbium]] was named for the village it was discovered in, so element 97 was named [[berkelium]].{{sfn|Weeks|Leichester|1968|p=848}} }} However, the element directly above element 98 in the periodic table, [[dysprosium]], has a name that means "hard to get at", so the researchers decided to set aside the informal naming convention.{{sfn|Heiserman|1992|p=347}} They added that "the best we can do is to point out [that] ... searchers a century ago found it difficult to get to California".{{sfn|Weeks|Leichester|1968|p=848}}
The discoverers named the new element after the university and the state. This was a break from the convention used for elements 95 to 97, which drew inspiration from how the elements directly above them in the periodic table were named.{{sfn|Weeks|Leichester|1968|p=849}}{{efn|[[Europium]], in the sixth period directly above element 95, was named for the continent it was discovered on, so element 95 was named [[americium]]. Element 96 was named [[curium]] for [[Marie Curie]] and [[Pierre Curie]] as an analog to the naming of [[gadolinium]], which was named for the scientist and engineer [[Johan Gadolin]]. [[Terbium]] was named for the village it was discovered in, so element 97 was named [[berkelium]].{{sfn|Weeks|Leichester|1968|p=848}} }} However, the element directly above element 98 in the periodic table, [[dysprosium]], has a name that means "hard to get at", so the researchers decided to set aside the informal naming convention.{{sfn|Heiserman|1992|p=347}} They added that "the best we can do is to point out [that] ... searchers a century ago found it difficult to get to California".{{sfn|Weeks|Leichester|1968|p=848}}


Weighable amounts of californium were first produced by the<!-- long duration -HOW LONG? --> irradiation of plutonium targets at [[Materials Testing Reactor]] at [[Idaho National Laboratory|National Reactor Testing Station]], [[eastern Idaho]]; these findings were reported in 1954.<ref>{{cite journal |journal=[[Physical Review]] |volume=94 |issue=4 |pages=1083 |date=1954 |author=Diamond, H. |title=Identification of Californium Isotopes 249, 250, 251, and 252 from Pile-Irradiated Plutonium |doi = 10.1103/PhysRev.94.1083 |bibcode = 1954PhRv...94.1083D |last2=Magnusson |first2=L. |last3=Mech |first3=J. |last4=Stevens |first4=C. |last5=Friedman |first5=A. |last6=Studier |first6=M. |last7=Fields |first7=P. |last8=Huizenga |first8=J. }}</ref> The high spontaneous fission rate of californium-252 was observed in these samples. The first experiment with californium in concentrated form occurred in 1958.{{sfn|Cunningham|1968|p=103}} The isotopes {{sup|249}}Cf to {{sup|252}}Cf were isolated that same year from a sample of [[plutonium-239]] that had been irradiated with neutrons in a nuclear reactor for five years.{{sfn|Jakubke|1994|p=166}} Two years later, in 1960, Burris Cunningham and James Wallman of Lawrence Radiation Laboratory of the University of California created the first californium compounds—californium trichloride, [[californium(III) oxychloride]], and californium oxide—by treating californium with steam and [[hydrochloric acid]].<ref>{{cite journal |journal = Science News Letter |volume = 78 |issue = 26 |date=December 1960 |title = Element 98 Prepared }}</ref>
Weighable amounts of californium were first produced by the<!-- long duration -HOW LONG? --> irradiation of plutonium targets at [[Materials Testing Reactor]] at [[Idaho National Laboratory|National Reactor Testing Station]], [[eastern Idaho]]; these findings were reported in 1954.<ref>{{cite journal |journal=[[Physical Review]] |volume=94 |issue=4 |page=1083 |date=1954 |author=Diamond, H. |title=Identification of Californium Isotopes 249, 250, 251, and 252 from Pile-Irradiated Plutonium |doi = 10.1103/PhysRev.94.1083 |bibcode = 1954PhRv...94.1083D |last2=Magnusson |first2=L. |last3=Mech |first3=J. |last4=Stevens |first4=C. |last5=Friedman |first5=A. |last6=Studier |first6=M. |last7=Fields |first7=P. |last8=Huizenga |first8=J. }}</ref> The high spontaneous fission rate of californium-252 was observed in these samples. The first experiment with californium in concentrated form occurred in 1958.{{sfn|Cunningham|1968|p=103}} The isotopes {{sup|249}}Cf to {{sup|252}}Cf were isolated that same year from a sample of [[plutonium-239]] that had been irradiated with neutrons in a nuclear reactor for five years.{{sfn|Jakubke|1994|p=166}} Two years later, in 1960, Burris Cunningham and James Wallman of Lawrence Radiation Laboratory of the University of California created the first californium compounds—californium trichloride, [[californium(III) oxychloride]], and californium oxide—by treating californium with steam and [[hydrochloric acid]].<ref>{{cite journal |journal = Science News Letter |volume = 78 |issue = 26 |date=December 1960 |title = Element 98 Prepared }}</ref>


The [[High Flux Isotope Reactor]] (HFIR) at ORNL in [[Oak Ridge, Tennessee]], started producing small batches of californium in the 1960s.<ref>{{cite web |url=http://web.ornl.gov/sci/rrd/pages/hfir.html |title=The High Flux Isotope Reactor |publisher=Oak Ridge National Laboratory |access-date=August 22, 2010 |archive-url=https://web.archive.org/web/20100527164346/http://web.ornl.gov/sci/rrd/pages/hfir.html <!--Added by H3llBot--> |archive-date=May 27, 2010 }}</ref> By 1995, HFIR nominally produced {{convert|500|mg|oz}} of californium annually.{{sfn|Osborne-Lee|1995|p=11}} Plutonium supplied by the United Kingdom to the United States under the [[1958 US–UK Mutual Defence Agreement]] was used for making californium.<ref>{{cite web |archive-url=https://web.archive.org/web/20061213032416/http://www.mod.uk/NR/rdonlyres/B31B4EF0-A584-4CC6-9B14-B5E89E6848F8/0/plutoniumandaldermaston.pdf |archive-date=December 13, 2006 |url=http://www.mod.uk/NR/rdonlyres/B31B4EF0-A584-4CC6-9B14-B5E89E6848F8/0/plutoniumandaldermaston.pdf |title=Plutonium and Aldermaston – an Historical Account |publisher=UK Ministry of Defence |date=September 4, 2001 |access-date=March 15, 2007|page=30 }}</ref>
The [[High Flux Isotope Reactor]] (HFIR) at ORNL in [[Oak Ridge, Tennessee]], started producing small batches of californium in the 1960s.<ref>{{cite web |url=http://web.ornl.gov/sci/rrd/pages/hfir.html |title=The High Flux Isotope Reactor |publisher=Oak Ridge National Laboratory |access-date=August 22, 2010 |archive-url=https://web.archive.org/web/20100527164346/http://web.ornl.gov/sci/rrd/pages/hfir.html <!--Added by H3llBot--> |archive-date=May 27, 2010 }}</ref> By 1995, HFIR nominally produced {{convert|500|mg|oz}} of californium annually.{{sfn|Osborne-Lee|1995|p=11}} Plutonium supplied by the United Kingdom to the United States under the [[1958 US–UK Mutual Defence Agreement]] was used for making californium.<ref>{{cite web |archive-url=https://web.archive.org/web/20061213032416/http://www.mod.uk/NR/rdonlyres/B31B4EF0-A584-4CC6-9B14-B5E89E6848F8/0/plutoniumandaldermaston.pdf |archive-date=December 13, 2006 |url=http://www.mod.uk/NR/rdonlyres/B31B4EF0-A584-4CC6-9B14-B5E89E6848F8/0/plutoniumandaldermaston.pdf |title=Plutonium and Aldermaston – an Historical Account |publisher=UK Ministry of Defence |date=September 4, 2001 |access-date=March 15, 2007|page=30 }}</ref>


The [[United States Atomic Energy Commission|Atomic Energy Commission]] sold {{sup|252}}Cf to industrial and academic customers in the early 1970s for $10/microgram,<ref name="osti" /> and an average of {{convert|150|mg|oz|abbr=on}} of {{sup|252}}Cf were shipped each year from 1970 to 1990.{{sfn|Osborne-Lee|1995|p=6}}{{efn|The [[Nuclear Regulatory Commission]] replaced the Atomic Energy Commission when the [[Energy Reorganization Act of 1974]] was implemented. The price of californium-252 was increased by the NRC several times and was $60 per microgram by 1999; this price does not include the cost of encapsulation and transportation.<ref name="osti" /> }} Californium metal was first prepared in 1974 by Haire and Baybarz, who reduced californium(III) oxide with lanthanum metal to obtain microgram amounts of sub-micrometer thick films.{{sfn|Haire|2006|p=1519}}<ref>{{cite journal |last1=Haire |first1=R. G. |last2=Baybarz |first2=R. D. |title=Crystal Structure and Melting Point of Californium Metal |journal=Journal of Inorganic and Nuclear Chemistry |volume=36 |issue=6 |pages=1295 |date=1974 |doi=10.1016/0022-1902(74)80067-9 }}</ref>{{efn|In 1975, another paper stated that the californium metal prepared the year before was the hexagonal compound Cf{{sub|2}}O{{sub|2}}S and face-centered cubic compound CfS.<ref>{{cite journal |doi=10.1016/0022-1902(75)80787-1 |journal=Journal of Inorganic and Nuclear Chemistry |date=1975 |pages=1441–1442 |volume=37 |issue=6 |title=On Californium Metal |last=Zachariasen |first=W. }}</ref> The 1974 work was confirmed in 1976 and work on californium metal continued.{{sfn|Haire|2006|p=1519}} }}
The [[United States Atomic Energy Commission|Atomic Energy Commission]] sold {{sup|252}}Cf to industrial and academic customers in the early 1970s for $10/microgram,<ref name="osti" /> and an average of {{convert|150|mg|oz|abbr=on}} of {{sup|252}}Cf were shipped each year from 1970 to 1990.{{sfn|Osborne-Lee|1995|p=6}}{{efn|The [[Nuclear Regulatory Commission]] replaced the Atomic Energy Commission when the [[Energy Reorganization Act of 1974]] was implemented. The price of californium-252 was increased by the NRC several times and was $60 per microgram by 1999; this price does not include the cost of encapsulation and transportation.<ref name="osti" /> }} Californium metal was first prepared in 1974 by Haire and Baybarz, who reduced californium(III) oxide with lanthanum metal to obtain microgram amounts of sub-micrometer thick films.{{sfn|Haire|2006|p=1519}}<ref>{{cite journal |last1=Haire |first1=R. G. |last2=Baybarz |first2=R. D. |title=Crystal Structure and Melting Point of Californium Metal |journal=Journal of Inorganic and Nuclear Chemistry |volume=36 |issue=6 |page=1295 |date=1974 |doi=10.1016/0022-1902(74)80067-9 }}</ref>{{efn|In 1975, another paper stated that the californium metal prepared the year before was the hexagonal compound Cf{{sub|2}}O{{sub|2}}S and face-centered cubic compound CfS.<ref>{{cite journal |doi=10.1016/0022-1902(75)80787-1 |journal=Journal of Inorganic and Nuclear Chemistry |date=1975 |pages=1441–1442 |volume=37 |issue=6 |title=On Californium Metal |last=Zachariasen |first=W. }}</ref> The 1974 work was confirmed in 1976 and work on californium metal continued.{{sfn|Haire|2006|p=1519}} }}


== Occurrence ==
== Occurrence ==
Traces of californium can be found near facilities that use the element in mineral prospecting and in medical treatments.{{sfn|Emsley|2001|p=90}} The element is fairly insoluble in water, but it adheres well to ordinary soil; and concentrations of it in the soil can be 500 times higher than in the water surrounding the soil particles.<ref name="ANL2005">{{cite web|url=http://www.evs.anl.gov/pub/doc/Californium.pdf |title=Human Health Fact Sheet: Californium |date=August 2005 |publisher=Argonne National Laboratory |url-status=dead |archive-url=https://web.archive.org/web/20110721032736/http://www.evs.anl.gov/pub/doc/Californium.pdf |archive-date=July 21, 2011 }}</ref>
Traces of californium can be found near facilities that use the element in mineral prospecting and in medical treatments.{{sfn|Emsley|2001|p=90}} The element is fairly insoluble in water, but it adheres well to ordinary soil; and concentrations of it in the soil can be 500 times higher than in the water surrounding the soil particles.<ref name="ANL2005">{{cite web|url=http://www.evs.anl.gov/pub/doc/Californium.pdf |title=Human Health Fact Sheet: Californium |date=August 2005 |publisher=Argonne National Laboratory |archive-url=https://web.archive.org/web/20110721032736/http://www.evs.anl.gov/pub/doc/Californium.pdf |archive-date=July 21, 2011 }}</ref>


[[Nuclear fallout]] from atmospheric [[nuclear weapons testing]] prior to 1980 contributed a small amount of californium to the environment.<ref name="ANL2005" /> Californium-249, -252, -253, and -254 have been observed in the radioactive dust collected from the air after a nuclear explosion.<ref>{{cite journal|title = Transplutonium Elements in Thermonuclear Test Debris|journal = Physical Review|date = 1956|volume = 102|issue = 1|pages = 180–182|doi = 10.1103/PhysRev.102.180|bibcode = 1956PhRv..102..180F|last1=Fields|first1=P. R.|last2 = Studier|first2 = M.|last3 = Diamond|first3 = H.|last4 = Mech|first4 = J.|last5 = Inghram|first5 = M.|last6 = Pyle|first6 = G.|last7 = Stevens|first7 = C.|last8 = Fried|first8 = S.|last9 = Manning|first9 = W.|display-authors=8}}</ref> Californium is not a major radionuclide at [[United States Department of Energy]] legacy sites since it was not produced in large quantities.<ref name="ANL2005" />
[[Nuclear fallout]] from atmospheric [[nuclear weapons testing]] prior to 1980 contributed a small amount of californium to the environment.<ref name="ANL2005" /> Californium-249, -252, -253, and -254 have been observed in the radioactive dust collected from the air after a nuclear explosion.<ref>{{cite journal|title = Transplutonium Elements in Thermonuclear Test Debris|journal = Physical Review|date = 1956|volume = 102|issue = 1|pages = 180–182|doi = 10.1103/PhysRev.102.180|bibcode = 1956PhRv..102..180F|last1=Fields|first1=P. R.|last2 = Studier|first2 = M.|last3 = Diamond|first3 = H.|last4 = Mech|first4 = J.|last5 = Inghram|first5 = M.|last6 = Pyle|first6 = G.|last7 = Stevens|first7 = C.|last8 = Fried|first8 = S.|last9 = Manning|first9 = W.|display-authors=8}}</ref> Californium is not a major radionuclide at [[United States Department of Energy]] legacy sites since it was not produced in large quantities.<ref name="ANL2005" />


Californium was once believed to be produced in [[supernova]]s, as their decay matches the 60-day half-life of {{sup|254}}Cf.<ref name="super1">{{cite journal|last=Baade|first=W.|author2=Burbidge, G. R.|author3=Hoyle, F.|author4=Burbidge, E. M.|author5=Christy, R. F.|author6=Fowler, W. A.|title=Supernovae and Californium 254|journal=Publications of the Astronomical Society of the Pacific|date=August 1956|volume=68|issue=403|pages=296–300|doi=10.1086/126941|url=http://authors.library.caltech.edu/6553/1/BURpr56.pdf |archive-url=https://ghostarchive.org/archive/20221010/http://authors.library.caltech.edu/6553/1/BURpr56.pdf |archive-date=2022-10-10 |url-status=live|access-date=September 26, 2012|bibcode = 1956PASP...68..296B |doi-access=free}}</ref> However, subsequent studies failed to demonstrate any californium spectra,<ref name="super2">{{cite journal|last=Conway|first=J. G.|author2=Hulet, E.K. |author3=Morrow, R.J. |title=Emission Spectrum of Californium|journal=Journal of the Optical Society of America|date=February 1, 1962|volume=52|issue=2|pages=222|doi=10.1364/josa.52.000222 |pmid=13881026|bibcode=1962JOSA...52..222C |osti=4806792|url=http://www.escholarship.org/uc/item/9c3297wf}}</ref> and supernova light curves are now thought to follow the decay of [[Isotopes of nickel|nickel-56]].{{sfn|Ruiz-Lapuente1996|p=274}}
Californium was once believed to be produced in [[supernova]]s, as their decay matches the 60-day half-life of {{sup|254}}Cf.<ref name="super1">{{cite journal|last=Baade|first=W.|author2=Burbidge, G. R.|author3=Hoyle, F.|author4=Burbidge, E. M.|author5=Christy, R. F.|author6=Fowler, W. A.|title=Supernovae and Californium 254|journal=Publications of the Astronomical Society of the Pacific|date=August 1956|volume=68|issue=403|pages=296–300|doi=10.1086/126941|url=http://authors.library.caltech.edu/6553/1/BURpr56.pdf |archive-url=https://ghostarchive.org/archive/20221010/http://authors.library.caltech.edu/6553/1/BURpr56.pdf |archive-date=2022-10-10 |url-status=live|access-date=September 26, 2012|bibcode = 1956PASP...68..296B |doi-access=free}}</ref> However, subsequent studies failed to demonstrate any californium spectra,<ref name="super2">{{cite journal|last=Conway|first=J. G.|author2=Hulet, E.K. |author3=Morrow, R.J. |title=Emission Spectrum of Californium|journal=Journal of the Optical Society of America|date=February 1, 1962|volume=52|issue=2|page=222|doi=10.1364/josa.52.000222 |pmid=13881026|bibcode=1962JOSA...52..222C |osti=4806792|url=http://www.escholarship.org/uc/item/9c3297wf}}</ref> and supernova light curves are now thought to follow the decay of [[Isotopes of nickel|nickel-56]].{{sfn|Ruiz-Lapuente1996|p=274}}


The [[transuranic element]]s up to [[fermium]], including californium, should have been present in the [[natural nuclear fission reactor]] at [[Oklo]], but no longer do so.<ref name="emsley">{{cite book|last=Emsley|first=John|title=Nature's Building Blocks: An A-Z Guide to the Elements|edition=New|date=2011|publisher=Oxford University Press|location=New York, NY|isbn=978-0-19-960563-7}}</ref>
The transuranic elements up to [[fermium]], including californium, should have been present in the [[natural nuclear fission reactor]] at [[Oklo]], but any quantities produced then would have long since decayed away.<ref name="emsley">{{cite book|last=Emsley|first=John|title=Nature's Building Blocks: An A-Z Guide to the Elements|edition=New|date=2011|publisher=Oxford University Press|location=New York, NY|isbn=978-0-19-960563-7}}</ref>


== Production ==
== Production ==
Line 102: Line 103:


== Applications ==
== Applications ==
[[File:CfShield.JPG|thumb|Fifty-ton shipping cask built at ORNL which can transport up to 1 gram of {{sup|252}}Cf.{{sfn|Seaborg|1994|p=245}} Large and heavily shielded transport containers are needed to prevent the release of highly radioactive material in case of normal and hypothetical accidents.<ref>{{cite web|url=http://rampac.energy.gov/PCN/EM-PCP-certified-pkgs-8808.pdf|title=DOE Certified Radioactive Materials Transportation Packagings|last=Shuler|first=James|date=2008|page=1|publisher=United States Department of Energy|access-date=April 7, 2011|archive-date=October 15, 2011|archive-url=https://web.archive.org/web/20111015040627/http://rampac.energy.gov/PCN/EM-PCP-certified-pkgs-8808.pdf|url-status=dead}}</ref>|alt= Large conical structure on a pulley with a man on top and two near the base.]]
[[File:CfShield.JPG|thumb|Fifty-ton shipping cask built at ORNL which can transport up to 1 gram of {{sup|252}}Cf.{{sfn|Seaborg|1994|p=245}} Large and heavily shielded transport containers are needed to prevent the release of highly radioactive material in case of normal and hypothetical accidents.<ref>{{cite web|url=http://rampac.energy.gov/PCN/EM-PCP-certified-pkgs-8808.pdf|title=DOE Certified Radioactive Materials Transportation Packagings|last=Shuler|first=James|date=2008|page=1|publisher=United States Department of Energy|access-date=April 7, 2011|archive-date=October 15, 2011|archive-url=https://web.archive.org/web/20111015040627/http://rampac.energy.gov/PCN/EM-PCP-certified-pkgs-8808.pdf}}</ref>|alt= Large conical structure on a pulley with a man on top and two near the base.]]


<!-- NEEDS CITE Californium is the heaviest metal known at this time that has a practical use outside of research laboratories; [[einsteinium]] and all other elements above it have sufficiently short half-lives that they have no use except the production of heavier elements.-->=== Neutron source ===
<!-- NEEDS CITE Californium is the heaviest metal known at this time that has a practical use outside of research laboratories; [[einsteinium]] and all other elements above it have sufficiently short half-lives that they have no use except the production of heavier elements.-->=== Neutron source ===
{{SimpleNuclide|Californium|252|link=yes}} has a number of specialized uses as a strong [[Neutron source|neutron emitter]]; it produces 139&nbsp;million neutrons per microgram per minute.<ref name="osti" /> This property makes it useful as a [[startup neutron source]] for some nuclear reactors{{sfn|O'Neil|2006|p=276}} and as a portable (non-reactor based) neutron source for [[neutron activation analysis]] to detect trace amounts of elements in samples.<ref name="Martin2000">{{cite conference|last=Martin |first=R. C. |title=Applications and Availability of Californium-252 Neutron Sources for Waste Characterization |date=September 24, 2000 |url=http://www.ornl.gov/~webworks/cpr/pres/107270_.pdf |access-date=May 2, 2010 |conference=Spectrum 2000 International Conference on Nuclear and Hazardous Waste Management |location=Chattanooga, Tennessee |url-status=dead |archive-url=https://web.archive.org/web/20100601160926/http://www.ornl.gov/~webworks/cpr/pres/107270_.pdf |archive-date=June 1, 2010 }}</ref>{{efn|By 1990, californium-252 had replaced plutonium-[[beryllium]] neutron sources due to its smaller size and lower heat and gas generation.{{sfn|Seaborg|1990|p=318}} }} Neutrons from californium are used as a treatment of certain [[Cervical cancer|cervical]] and [[brain tumor|brain cancers]] where other [[radiation therapy]] is ineffective.{{sfn|O'Neil|2006|p=276}} It has been used in educational applications since 1969 when [[Georgia Tech|Georgia Institute of Technology]] got a loan of 119&nbsp;μg of {{sup|252}}Cf from the [[Savannah River Site]].{{sfn|Osborne-Lee|1995|p=33}} It is also used with online elemental [[coal analyzer]]s and [[bulk material analyzer]]s in the coal and cement industries.
{{SimpleNuclide|Californium|252|link=yes}} has a number of specialized uses as a strong [[Neutron source|neutron emitter]]; it produces 139&nbsp;million neutrons per microgram per minute.<ref name="osti" /> This property makes it useful as a [[startup neutron source]] for some nuclear reactors{{sfn|O'Neil|2006|p=276}} and as a portable (non-reactor based) neutron source for [[neutron activation analysis]] to detect trace amounts of elements in samples.<ref name="Martin2000">{{cite conference|last=Martin |first=R. C. |title=Applications and Availability of Californium-252 Neutron Sources for Waste Characterization |date=September 24, 2000 |url=http://www.ornl.gov/~webworks/cpr/pres/107270_.pdf |access-date=May 2, 2010 |conference=Spectrum 2000 International Conference on Nuclear and Hazardous Waste Management |location=Chattanooga, Tennessee |archive-url=https://web.archive.org/web/20100601160926/http://www.ornl.gov/~webworks/cpr/pres/107270_.pdf |archive-date=June 1, 2010 }}</ref>{{efn|By 1990, californium-252 had replaced plutonium-[[beryllium]] neutron sources due to its smaller size and lower heat and gas generation.{{sfn|Seaborg|1990|p=318}} }} Neutrons from californium are used as a treatment of certain [[Cervical cancer|cervical]] and [[brain tumor|brain cancers]] where other [[radiation therapy]] is ineffective.{{sfn|O'Neil|2006|p=276}} It has been used in educational applications since 1969 when [[Georgia Tech|Georgia Institute of Technology]] got a loan of 119&nbsp;μg of {{sup|252}}Cf from the [[Savannah River Site]].{{sfn|Osborne-Lee|1995|p=33}} It is also used with online elemental [[coal analyzer]]s and [[bulk material analyzer]]s in the coal and cement industries.


Neutron penetration into materials makes californium useful in detection instruments such as [[fuel rod]] scanners;{{sfn|O'Neil|2006|p=276}} [[Neutron imaging#Neutron radiography (film)|neutron radiography]] of aircraft and weapons components to detect [[corrosion]], bad welds, cracks and trapped moisture;{{sfn|Osborne-Lee|1995|pp=26–27}}<!-- NEEDS CITE in airport [[prompt gamma neutron activation analysis|neutron-activation]] detectors of explosives, --> and in portable metal detectors.<ref>{{cite web|url=http://www.pnl.gov/news/2000/00-43.htm|title=Will You be 'Mine'? Physics Key to Detection|date=October 25, 2000|publisher = Pacific Northwest National Laboratory|access-date = March 21, 2007 |archive-url = https://web.archive.org/web/20070218125029/http://www.pnl.gov/news/2000/00-43.htm <!-- Bot retrieved archive --> |archive-date = February 18, 2007 }}</ref> [[Neutron moisture gauge]]s use {{sup|252}}Cf to find water and petroleum layers in oil wells, as a portable [[neutron source]] for gold and silver prospecting for on-the-spot analysis,{{sfn|CRC|2006|p=4.8}} and to detect ground water movement.<ref>{{cite journal|journal = Ground Water|volume = 18|issue = 1|pages =14–23|date = 2006|title =Ground-Water Tracers – A Short Review|author = Davis, S. N. |doi = 10.1111/j.1745-6584.1980.tb03366.x|last2 = Thompson|first2 = Glenn M.|last3 = Bentley|first3 = Harold W.|last4 = Stiles|first4 = Gary }}</ref> The main uses of {{sup|252}}Cf in 1982 were, reactor start-up (48.3%), fuel rod scanning (25.3%), and activation analysis (19.4%).{{sfn|Osborne-Lee|1995|p=12}} By 1994, most {{sup|252}}Cf was used in neutron radiography (77.4%), with fuel rod scanning (12.1%) and reactor start-up (6.9%) as important but secondary uses.{{sfn|Osborne-Lee|1995|p=12}} In 2021, fast neutrons from {{sup|252}}Cf were used for wireless data transmission.<ref>{{cite journal|journal = Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment|volume = 1021|issue = 1|pages = 165946|date = 2022|title = Wireless information transfer with fast neutrons|author = Joyce, Malcolm J.|last2 = Aspinall|first2 = Michael D.|last3 = Clark|first3 = Mackenzie|last4 = Dale|first4 = Edward|last5 = Nye|first5 = Hamish|last6 = Parker|first6 = Andrew|last7 = Snoj|first7 = Luka|last8 = Spires|first8 = Joe|doi = 10.1016/j.nima.2021.165946| bibcode=2022NIMPA102165946J | s2cid=240341300 |issn=0168-9002 |doi-access = free}}</ref>
Neutron penetration into materials makes californium useful in detection instruments such as [[fuel rod]] scanners;{{sfn|O'Neil|2006|p=276}} [[Neutron imaging#Neutron radiography (film)|neutron radiography]] of aircraft and weapons components to detect [[corrosion]], bad welds, cracks and trapped moisture;{{sfn|Osborne-Lee|1995|pp=26–27}}<!-- NEEDS CITE in airport [[prompt gamma neutron activation analysis|neutron-activation]] detectors of explosives, --> and in portable metal detectors.<ref>{{cite web|url=http://www.pnl.gov/news/2000/00-43.htm|title=Will You be 'Mine'? Physics Key to Detection|date=October 25, 2000|publisher = Pacific Northwest National Laboratory|access-date = March 21, 2007 |archive-url = https://web.archive.org/web/20070218125029/http://www.pnl.gov/news/2000/00-43.htm <!-- Bot retrieved archive --> |archive-date = February 18, 2007 }}</ref> [[Neutron moisture gauge]]s use {{sup|252}}Cf to find water and petroleum layers in oil wells, as a portable [[neutron source]] for gold and silver prospecting for on-the-spot analysis,{{sfn|CRC|2006|p=4.8}} and to detect ground water movement.<ref>{{cite journal|journal = Ground Water|volume = 18|issue = 1|pages =14–23|date = 2006|title =Ground-Water Tracers – A Short Review|author = Davis, S. N. |doi = 10.1111/j.1745-6584.1980.tb03366.x|last2 = Thompson|first2 = Glenn M.|last3 = Bentley|first3 = Harold W.|last4 = Stiles|first4 = Gary }}</ref> The main uses of {{sup|252}}Cf in 1982 were, reactor start-up (48.3%), fuel rod scanning (25.3%), and activation analysis (19.4%).{{sfn|Osborne-Lee|1995|p=12}} By 1994, most {{sup|252}}Cf was used in neutron radiography (77.4%), with fuel rod scanning (12.1%) and reactor start-up (6.9%) as important but secondary uses.{{sfn|Osborne-Lee|1995|p=12}} In 2021, fast neutrons from {{sup|252}}Cf were used for wireless data transmission.<ref>{{cite journal|journal = Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment|volume = 1021|issue = 1|article-number = 165946|date = 2022|title = Wireless information transfer with fast neutrons|author = Joyce, Malcolm J.|last2 = Aspinall|first2 = Michael D.|last3 = Clark|first3 = Mackenzie|last4 = Dale|first4 = Edward|last5 = Nye|first5 = Hamish|last6 = Parker|first6 = Andrew|last7 = Snoj|first7 = Luka|last8 = Spires|first8 = Joe|doi = 10.1016/j.nima.2021.165946| bibcode=2022NIMPA102165946J | s2cid=240341300 |issn=0168-9002 |doi-access = free}}</ref>


=== Superheavy element production ===
=== Superheavy element production ===
{{See also|Superheavy element#Synthesis of superheavy nuclei}}
{{See also|Superheavy element#Synthesis of superheavy nuclei}}
In October 2006, researchers announced that three atoms of [[oganesson]] (element 118) had been identified at [[Joint Institute for Nuclear Research]] in [[Dubna]], [[Russia]], from bombarding {{sup|249}}Cf with [[calcium-48]], making it the heaviest element ever made. The target contained about 10&nbsp;mg of {{sup|249}}Cf deposited on a titanium foil of 32&nbsp;cm{{sup|2}} area.<ref>{{cite journal |title = Synthesis of the isotopes of elements 118 and 116 in the californium-249 and <sup>245</sup>Cm+<sup>48</sup>Ca fusion reactions |journal = Physical Review C |date = 2006 |volume = 74 |issue =4 |pages = 044602–044611 |doi = 10.1103/PhysRevC.74.044602 |bibcode=2006PhRvC..74d4602O |last1=Oganessian |first1=Yu. Ts. |last2=Utyonkov |first2=V. |last3=Lobanov |first3=Yu. |last4=Abdullin |first4=F. |last5=Polyakov |first5=A. |last6=Sagaidak |first6=R. |last7=Shirokovsky |first7=I. |last8=Tsyganov |first8=Yu. |last9=Voinov |first9=A. |display-authors=8 |doi-access=free}}</ref><ref>{{cite journal |author = Sanderson, K. |title = Heaviest element made – again |journal = Nature News |publisher =Nature |date = October 17, 2006 |doi=10.1038/news061016-4 |s2cid = 121148847}}</ref><ref>{{cite web|author=Schewe, P. |author2=Stein, B. |title=Elements 116 and 118 Are Discovered |work=Physics News Update |publisher=American Institute of Physics |date=October 17, 2006 |url=http://www.aip.org/pnu/2006/797.html |access-date=October 19, 2006 |url-status=dead |archive-url=https://web.archive.org/web/20061026072537/http://www.aip.org/pnu/2006/797.html |archive-date=October 26, 2006 }}</ref> <!-- EXPLAIN Calibration, [[dosimetry]], and fission fragment and half-life studies are other applications of californium.{{sfn|Osborne-Lee|1995|p=34}} --> Californium has also been used to produce other transuranic elements; for example, [[lawrencium]] was first synthesized in 1961 by bombarding californium with [[boron]] nuclei.<ref>{{cite journal|title = Element 103 Synthesized|journal = Science News-Letter|volume = 79|issue = 17|date=April 1961|page = 259|doi = 10.2307/3943043|author1 = <Please add first missing authors to populate metadata.> |jstor = 3943043}}</ref>
In October 2006, researchers announced that three atoms of [[oganesson]] (element 118) had been identified at [[Joint Institute for Nuclear Research]] in [[Dubna]], [[Russia]], from bombarding {{sup|249}}Cf with [[calcium-48]], making it the heaviest element ever made. The target contained about 10&nbsp;mg of {{sup|249}}Cf deposited on a titanium foil of 32&nbsp;cm{{sup|2}} area.<ref>{{cite journal |title = Synthesis of the isotopes of elements 118 and 116 in the californium-249 and <sup>245</sup>Cm+<sup>48</sup>Ca fusion reactions |journal = Physical Review C |date = 2006 |volume = 74 |issue =4 |pages = 044602–044611 |doi = 10.1103/PhysRevC.74.044602 |bibcode=2006PhRvC..74d4602O |last1=Oganessian |first1=Yu. Ts. |last2=Utyonkov |first2=V. |last3=Lobanov |first3=Yu. |last4=Abdullin |first4=F. |last5=Polyakov |first5=A. |last6=Sagaidak |first6=R. |last7=Shirokovsky |first7=I. |last8=Tsyganov |first8=Yu. |last9=Voinov |first9=A. |display-authors=8 |doi-access=free}}</ref><ref>{{cite journal |author = Sanderson, K. |title = Heaviest element made – again |journal = Nature News |publisher =Nature |date = October 17, 2006 |doi=10.1038/news061016-4 |s2cid = 121148847}}</ref><ref>{{cite web|author=Schewe, P. |author2=Stein, B. |title=Elements 116 and 118 Are Discovered |work=Physics News Update |publisher=American Institute of Physics |date=October 17, 2006 |url=http://www.aip.org/pnu/2006/797.html |access-date=October 19, 2006 |archive-url=https://web.archive.org/web/20061026072537/http://www.aip.org/pnu/2006/797.html |archive-date=October 26, 2006 }}</ref> <!-- EXPLAIN Calibration, [[dosimetry]], and fission fragment and half-life studies are other applications of californium.{{sfn|Osborne-Lee|1995|p=34}} --> Californium has also been used to produce other transuranic elements; for example, [[lawrencium]] was first synthesized in 1961 by bombarding californium with [[boron]] nuclei.<ref>{{cite journal|title = Element 103 Synthesized|journal = Science News-Letter|volume = 79|issue = 17|date=April 1961|page = 259|doi = 10.2307/3943043|author1 = <Please add first missing authors to populate metadata.> |jstor = 3943043}}</ref>


=== Hypothetical nuclear weapons ===
=== Hypothetical nuclear weapons ===
{{See also|Nuclear weapon design#Minor actinide fission weapons}}
{{See also|Nuclear weapon design#Minor actinide fission weapons}}
{{SimpleNuclide|Californium|251|link=yes}} has a very small calculated [[critical mass]] of about {{convert|5|kg|0|abbr=on}},<ref>{{cite web |title=Evaluation of nuclear criticality safety data and limits for actinides in transport |url=http://ec.europa.eu/energy/nuclear/transport/doc/irsn_sect03_146.pdf |url-status=dead |archive-url=https://web.archive.org/web/20110519171204/http://ec.europa.eu/energy/nuclear/transport/doc/irsn_sect03_146.pdf |archive-date=May 19, 2011 |access-date=December 20, 2010 |publisher=Institut de Radioprotection et de Sûreté Nucléaire |page=16}}</ref> high lethality, and a relatively short period of toxic environmental irradiation. The low critical mass of californium led to some exaggerated claims about possible uses for the element.{{efn|An article entitled "Facts and Fallacies of World War III" in the July 1961 edition of ''[[Popular Science]]'' magazine read "A californium atomic bomb need be no bigger than a pistol bullet. You could build a hand-held six-shooter to fire bullets that would explode on contact with the force of 10 tons of TNT."<ref>{{cite journal|journal=[[Popular Science]]|pages= 92–95, 178–181|date=July 1961|volume=179|issue=1|issn=0161-7370|title=Facts and Fallacies of World War III|url=https://books.google.com/books?id=OiEDAAAAMBAJ&pg=PA180|author1=Mann, Martin}}"force of 10 tons of TNT" on page 180.</ref>}}
{{SimpleNuclide|Californium|251|link=yes}} has a very small calculated [[critical mass]] of about {{convert|5|kg|0|abbr=on}},<ref>{{cite web |title=Evaluation of nuclear criticality safety data and limits for actinides in transport |url=http://ec.europa.eu/energy/nuclear/transport/doc/irsn_sect03_146.pdf |archive-url=https://web.archive.org/web/20110519171204/http://ec.europa.eu/energy/nuclear/transport/doc/irsn_sect03_146.pdf |archive-date=May 19, 2011 |access-date=December 20, 2010 |publisher=Institut de Radioprotection et de Sûreté Nucléaire |page=16}}</ref> high lethality, and a relatively short period of toxic environmental irradiation. The low critical mass of californium led to some exaggerated claims about possible uses for the element.{{efn|An article entitled "Facts and Fallacies of World War III" in the July 1961 edition of ''[[Popular Science]]'' magazine read "A californium atomic bomb need be no bigger than a pistol bullet. You could build a hand-held six-shooter to fire bullets that would explode on contact with the force of 10 tons of TNT."<ref>{{cite journal|journal=[[Popular Science]]|pages= 92–95, 178–181|date=July 1961|volume=179|issue=1|issn=0161-7370|title=Facts and Fallacies of World War III|url=https://books.google.com/books?id=OiEDAAAAMBAJ&pg=PA180|author1=Mann, Martin}}"force of 10 tons of TNT" on page 180.</ref>}}


== Precautions ==
== Precautions ==
Line 371: Line 372:
* [http://www.periodicvideos.com/videos/098.htm Californium] at ''[[The Periodic Table of Videos]]'' (University of Nottingham)
* [http://www.periodicvideos.com/videos/098.htm Californium] at ''[[The Periodic Table of Videos]]'' (University of Nottingham)
* [http://www.nuclearweaponarchive.org/Nwfaq/Nfaq6.html#nfaq6.2 NuclearWeaponArchive.org – Californium]
* [http://www.nuclearweaponarchive.org/Nwfaq/Nfaq6.html#nfaq6.2 NuclearWeaponArchive.org – Californium]
* [http://toxnet.nlm.nih.gov/cgi-bin/sis/search/r?dbs+hsdb:@term+@rel+@na+californium,radioactive Hazardous Substances Databank – Californium, Radioactive]
* [https://www.nlm.nih.gov/toxnet/index.html Hazardous Substances Databank – Californium, Radioactive]


{{Periodic table (navbox)}}
{{Periodic table (navbox)}}

Latest revision as of 15:10, 1 October 2025

Script error: No such module "about". Template:Use mdy dates Template:Main other Template:Infobox californium Californium is a synthetic chemical element; it has symbol Cf and atomic number 98. It was first synthesized in 1950 at Lawrence Berkeley National Laboratory (then the University of California Radiation Laboratory) by bombarding curium with alpha particles (helium-4 ions). It is an actinide element, the sixth transuranium element to be synthesized, and has the second-highest atomic mass of all elements that have been produced in amounts large enough to see with the naked eye (after einsteinium). It was named after the university and the U.S. state of California.

Two crystalline forms exist at normal pressure: one above and one below Template:Convert. A third form exists at high pressure. Californium slowly tarnishes in air at room temperature. Californium compounds are dominated by the +3 oxidation state. The most stable of californium's twenty known isotopes is californium-251, with a half-life of 898 years. This short half-life means the element is not found in significant quantities in the Earth's crust.Template:Efn 252Cf, with a half-life of about 2.645 years, is the most common isotope used and is produced at Oak Ridge National Laboratory (ORNL) in the United States and Research Institute of Atomic Reactors in Russia.

Californium is one of the few transuranium elements with practical uses. Most of these applications exploit the fact that certain isotopes of californium emit neutrons. For example, californium can be used to help start up nuclear reactors, and it is used as a source of neutrons when studying materials using neutron diffraction and neutron spectroscopy. It can also be used in nuclear synthesis of higher mass elements; oganesson (element 118) was synthesized by bombarding californium-249 atoms with calcium-48 ions. Users of californium must take into account radiological concerns and the element's ability to disrupt the formation of red blood cells by bioaccumulating in skeletal tissue.

Characteristics

Physical properties

Californium is a silvery-white actinide metalTemplate:Sfn with a melting point of Template:Convert and an estimated boiling point of Template:Convert.Template:Sfn The pure metal is malleable and is easily cut with a knife. Californium metal starts to vaporize above Template:Convert when exposed to a vacuum.Template:Sfn Below Template:Convert californium metal is either ferromagnetic or ferrimagnetic (it acts like a magnet), between 48 and 66 K it is antiferromagnetic (an intermediate state), and above Template:Convert it is paramagnetic (external magnetic fields can make it magnetic).Template:Sfn It forms alloys with lanthanide metals but little is known about the resulting materials.Template:Sfn

The element has two crystalline forms at standard atmospheric pressure: a double-hexagonal close-packed form dubbed alpha (α) and a face-centered cubic form designated beta (β).Template:Efn The α form exists below 600–800 °C with a density of 15.10 g/cm3 and the β form exists above 600–800 °C with a density of 8.74 g/cm3.Template:Sfn At 48 GPa of pressure the β form changes into an orthorhombic crystal system due to delocalization of the atom's 5f electrons, which frees them to bond.Template:SfnTemplate:Efn

The bulk modulus of a material is a measure of its resistance to uniform pressure. Californium's bulk modulus is Template:Val, which is similar to trivalent lanthanide metals but smaller than more familiar metals, such as aluminium (70 GPa).Template:Sfn

Chemical properties and compounds

Script error: No such module "labelled list hatnote".

Representative californium compoundsTemplate:SfnTemplate:Efn
state compound formula color
+2 californium(II) bromide CfBr2 yellow
+2 californium(II) iodide CfI2 dark violet
+3 californium(III) oxide Cf2O3 yellow-green
+3 californium(III) fluoride CfF3 bright green
+3 californium(III) chloride CfCl3 emerald green
+3 californium(III) bromide CfBr3 yellowish green
+3 californium(III) iodide CfI3 lemon yellow
+3 californium(III) polyborate Cf[B6O8(OH)5] pale green
+4 californium(IV) oxide CfO2 black brown
+4 californium(IV) fluoride CfF4 green

Californium exhibits oxidation states of 4, 3, or 2. It typically forms eight or nine bonds to surrounding atoms or ions. Its chemical properties are predicted to be similar to other primarily 3+ valence actinide elementsTemplate:Sfn and the element dysprosium, which is the lanthanide above californium in the periodic table.Template:Sfn Compounds in the +4 oxidation state are strong oxidizing agents and those in the +2 state are strong reducing agents.Template:Sfn

The element slowly tarnishes in air at room temperature, with the rate increasing when moisture is added.Template:Sfn Californium reacts when heated with hydrogen, nitrogen, or a chalcogen (oxygen family element); reactions with dry hydrogen and aqueous mineral acids are rapid.Template:Sfn

Californium is only water-soluble as the californium(III) cation. Attempts to reduce or oxidize the +3 ion in solution have failed.Template:Sfn The element forms a water-soluble chloride, nitrate, perchlorate, and sulfate and is precipitated as a fluoride, oxalate, or hydroxide.Template:Sfn Californium is the heaviest actinide to exhibit covalent properties, as is observed in the californium borate.[1]

Isotopes

Script error: No such module "Labelled list hatnote".

All nuclear data not otherwise stated is from the standard source:[2]

Twenty isotopes of californium are known with mass number ranging from 237 to 256; the most stable are 251Cf with half-life 898 years, 249Cf with half-life 351 years, 250Cf at 13.08 years, and 252Cf at 2.645 years. All other isotopes have half-life shorter than a year, and most of these have half-lives less than 20 minutes.

249Cf is formed by beta decay of berkelium-249, and heavier californium isotopes are made by subjecting berkelium to intense neutron radiation in a nuclear reactor. Though californium-251 has the longest half-life, its production yield is relatively low due to its rapid depletion by reaction with another neutron (high neutron cross section).Template:Sfn

252Cf is a very strong neutron emitter, which makes it an extremely hazardous radioactive isotope.[3][4][5] 252Cf, 96.9% of the time, alpha decays to curium-248; the other 3.1% of decays are spontaneous fission. One microgram of 252Cf emits 2.3 million neutrons per second (about 3.7 neutrons per fission).[6] The other main isotopes of californium (248-251) also alpha decay to those of curium, with a much smaller fraction of fission.

History

Large pieces of equipment with a man standing nearby.
The Template:Convert cyclotron used to first synthesize californium

Californium was first made at University of California Radiation Laboratory, Berkeley, by physics researchers Stanley Gerald Thompson, Kenneth Street Jr., Albert Ghiorso, and Glenn T. Seaborg, about February 9, 1950.Template:Sfn It was the sixth transuranium element to be discovered; the team announced its discovery on March 17, 1950.[7][8]

To produce californium, a microgram-size target of curium-242 (Template:Nuclide) was bombarded with 35 MeV alpha particles (Template:Nuclide) in the Template:Convert cyclotron at Berkeley, which produced californium-245 (Template:Nuclide) plus one free neutron (Template:SubatomicParticle).Template:Sfn[7]

Template:Nuclide + Template:NuclideTemplate:Nuclide + Template:SuTemplate:SubatomicParticle

To identify and separate out the element, ion exchange and adsorsion methods were undertaken.[7][9] Only about 5,000 atoms of californium were produced in this experiment,Template:Sfn and these atoms had a half-life of 44 minutes.Template:Sfn

The discoverers named the new element after the university and the state. This was a break from the convention used for elements 95 to 97, which drew inspiration from how the elements directly above them in the periodic table were named.Template:SfnTemplate:Efn However, the element directly above element 98 in the periodic table, dysprosium, has a name that means "hard to get at", so the researchers decided to set aside the informal naming convention.Template:Sfn They added that "the best we can do is to point out [that] ... searchers a century ago found it difficult to get to California".Template:Sfn

Weighable amounts of californium were first produced by the irradiation of plutonium targets at Materials Testing Reactor at National Reactor Testing Station, eastern Idaho; these findings were reported in 1954.[10] The high spontaneous fission rate of californium-252 was observed in these samples. The first experiment with californium in concentrated form occurred in 1958.Template:Sfn The isotopes 249Cf to 252Cf were isolated that same year from a sample of plutonium-239 that had been irradiated with neutrons in a nuclear reactor for five years.Template:Sfn Two years later, in 1960, Burris Cunningham and James Wallman of Lawrence Radiation Laboratory of the University of California created the first californium compounds—californium trichloride, californium(III) oxychloride, and californium oxide—by treating californium with steam and hydrochloric acid.[11]

The High Flux Isotope Reactor (HFIR) at ORNL in Oak Ridge, Tennessee, started producing small batches of californium in the 1960s.[12] By 1995, HFIR nominally produced Template:Convert of californium annually.Template:Sfn Plutonium supplied by the United Kingdom to the United States under the 1958 US–UK Mutual Defence Agreement was used for making californium.[13]

The Atomic Energy Commission sold 252Cf to industrial and academic customers in the early 1970s for $10/microgram,[6] and an average of Template:Convert of 252Cf were shipped each year from 1970 to 1990.Template:SfnTemplate:Efn Californium metal was first prepared in 1974 by Haire and Baybarz, who reduced californium(III) oxide with lanthanum metal to obtain microgram amounts of sub-micrometer thick films.Template:Sfn[14]Template:Efn

Occurrence

Traces of californium can be found near facilities that use the element in mineral prospecting and in medical treatments.Template:Sfn The element is fairly insoluble in water, but it adheres well to ordinary soil; and concentrations of it in the soil can be 500 times higher than in the water surrounding the soil particles.[15]

Nuclear fallout from atmospheric nuclear weapons testing prior to 1980 contributed a small amount of californium to the environment.[15] Californium-249, -252, -253, and -254 have been observed in the radioactive dust collected from the air after a nuclear explosion.[16] Californium is not a major radionuclide at United States Department of Energy legacy sites since it was not produced in large quantities.[15]

Californium was once believed to be produced in supernovas, as their decay matches the 60-day half-life of 254Cf.[17] However, subsequent studies failed to demonstrate any californium spectra,[18] and supernova light curves are now thought to follow the decay of nickel-56.Template:Sfn

The transuranic elements up to fermium, including californium, should have been present in the natural nuclear fission reactor at Oklo, but any quantities produced then would have long since decayed away.[19]

Production

Script error: No such module "Labelled list hatnote". Californium is produced in nuclear reactors and particle accelerators.Template:Sfn Californium-250 is made by bombarding berkelium-249 (249Bk) with neutrons, forming berkelium-250 (250Bk) via neutron capture (n,γ) which, in turn, quickly beta decays) to californium-250 (250Cf) in the following reaction:Template:Sfn

Template:Nuclide(n,γ)Template:NuclideTemplate:Nuclide + β

Bombardment of 250Cf with neutrons produces 251Cf and 252Cf.Template:Sfn

Prolonged irradiation of americium, curium, and plutonium with neutrons produces milligram amounts of 252Cf and microgram amounts of 249Cf.Template:Sfn As of 2006, curium isotopes 244 to 248 are irradiated by neutrons in special reactors to produce mainly californium-252 with lesser amounts of isotopes 249 to 255.Template:Sfn

Microgram quantities of 252Cf are available for commercial use through the U.S. Nuclear Regulatory Commission.Template:Sfn Only two sites produce 252Cf: Oak Ridge National Laboratory in the U.S., and the Research Institute of Atomic Reactors in Dimitrovgrad, Russia. As of 2003, the two sites produce 0.25 grams and 0.025 grams of 252Cf per year, respectively.Template:Sfn

Three californium isotopes with significant half-lives are produced, requiring a total of 15 neutron captures by uranium-238 without nuclear fission or alpha decay occurring during the process.Template:Sfn 253Cf is at the end of a production chain that starts with uranium-238, and includes several isotopes of plutonium, americium, curium, and berkelium, and the californium isotopes 249 to 253 (see diagram).

A complex flow diagram showing various isotopes.
Scheme of the production of californium-252 from uranium-238 by neutron irradiation

Applications

Large conical structure on a pulley with a man on top and two near the base.
Fifty-ton shipping cask built at ORNL which can transport up to 1 gram of 252Cf.Template:Sfn Large and heavily shielded transport containers are needed to prevent the release of highly radioactive material in case of normal and hypothetical accidents.[20]

Neutron source

Template:SimpleNuclide has a number of specialized uses as a strong neutron emitter; it produces 139 million neutrons per microgram per minute.[6] This property makes it useful as a startup neutron source for some nuclear reactorsTemplate:Sfn and as a portable (non-reactor based) neutron source for neutron activation analysis to detect trace amounts of elements in samples.[21]Template:Efn Neutrons from californium are used as a treatment of certain cervical and brain cancers where other radiation therapy is ineffective.Template:Sfn It has been used in educational applications since 1969 when Georgia Institute of Technology got a loan of 119 μg of 252Cf from the Savannah River Site.Template:Sfn It is also used with online elemental coal analyzers and bulk material analyzers in the coal and cement industries.

Neutron penetration into materials makes californium useful in detection instruments such as fuel rod scanners;Template:Sfn neutron radiography of aircraft and weapons components to detect corrosion, bad welds, cracks and trapped moisture;Template:Sfn and in portable metal detectors.[22] Neutron moisture gauges use 252Cf to find water and petroleum layers in oil wells, as a portable neutron source for gold and silver prospecting for on-the-spot analysis,Template:Sfn and to detect ground water movement.[23] The main uses of 252Cf in 1982 were, reactor start-up (48.3%), fuel rod scanning (25.3%), and activation analysis (19.4%).Template:Sfn By 1994, most 252Cf was used in neutron radiography (77.4%), with fuel rod scanning (12.1%) and reactor start-up (6.9%) as important but secondary uses.Template:Sfn In 2021, fast neutrons from 252Cf were used for wireless data transmission.[24]

Superheavy element production

Script error: No such module "Labelled list hatnote". In October 2006, researchers announced that three atoms of oganesson (element 118) had been identified at Joint Institute for Nuclear Research in Dubna, Russia, from bombarding 249Cf with calcium-48, making it the heaviest element ever made. The target contained about 10 mg of 249Cf deposited on a titanium foil of 32 cm2 area.[25][26][27] Californium has also been used to produce other transuranic elements; for example, lawrencium was first synthesized in 1961 by bombarding californium with boron nuclei.[28]

Hypothetical nuclear weapons

Script error: No such module "Labelled list hatnote". Template:SimpleNuclide has a very small calculated critical mass of about Template:Convert,[29] high lethality, and a relatively short period of toxic environmental irradiation. The low critical mass of californium led to some exaggerated claims about possible uses for the element.Template:Efn

Precautions

Californium that bioaccumulates in skeletal tissue releases radiation that disrupts the body's ability to form red blood cells.Template:Sfn The element plays no natural biological role in any organism due to its intense radioactivity and low concentration in the environment.Template:Sfn

Californium can enter the body from ingesting contaminated food or drinks or by breathing air with suspended particles of the element. Once in the body, only 0.05% of the californium will reach the bloodstream. About 65% of that californium will be deposited in the skeleton, 25% in the liver, and the rest in other organs, or excreted, mainly in urine. Half of the californium deposited in the skeleton and liver are gone in 50 and 20 years, respectively. Californium in the skeleton adheres to bone surfaces before slowly migrating throughout the bone.[15]

The element is most dangerous if taken into the body. In addition, californium-249 and californium-251 can cause tissue damage externally, through gamma ray emission. Ionizing radiation emitted by californium on bone and in the liver can cause cancer.[15]

Notes

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References

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Bibliography

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External links

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