|
|
| Appearance |
| silvery |
| General properties |
| Name, symbol, number |
californium, Cf, 98 |
| Element category |
actinide |
| Group, period, block |
n/a, 7, f |
| Standard atomic weight |
(251) g·mol−1 |
| Electron configuration |
[Rn] 5f10 7s2 |
| Electrons per shell |
2, 8, 18, 32, 28, 8, 2 (Image) |
| Physical properties |
| Phase |
solid |
| Density (near r.t.) |
15.1 g·cm−3 |
| Melting point |
1173 K, 900 °C, 1652 °F |
| Boiling point |
1743 K, 1470 °C, 2678 °F |
| Atomic properties |
| Oxidation states |
2, 3, 4 |
| Electronegativity |
1.3 (Pauling scale) |
| Ionization energies |
1st: 608 kJ·mol−1 |
| Miscellanea |
| CAS registry number |
7440-71-3 |
| Most stable isotopes |
| Main article: Isotopes of californium |
|
|
|
|
Californium (pronounced /ˌkælɨˈfɔrniəm/, KAL-ə-FOR-nee-əm) is a metallic chemical element with the symbol Cf and atomic number 98. A radioactive transuranic element, californium is used in starting nuclear reactors, optimizing coal-fired power plants and cement production facilities (via online analyzers), medical treatment of cancer, and oil exploration via down hole well logging. It was first produced by bombarding curium with alpha particles (helium ions).
History
Californium was first synthesized at the University of California, Berkeley by researchers Stanley G. Thompson, Kenneth Street, Jr., Albert Ghiorso and Glenn T. Seaborg in 1950. It was the sixth transuranium element to be discovered and the team announced their discovery on March 17, 1950.[1][2][3] They named it after the U.S. state of California and the University of California, Berkeley. Unlike the names for the elements 95 to 97, this name did not reflect the chemical homology of element 98 to its corresponding sixth-period element, dysprosium (No. 66).[2]
To produce element 98, the team bombarded a microgram-sized target of 242Cm with 35 MeV alpha particles in the 60-inch (1.52 m) Berkeley cyclotron, which produced atoms of 245Cf (half-life 44 minutes) and a free neutron.
- 24296Cm + 42He → 24598Cf + 10n
Elutioncurves:
chromatographic separation of Dy, Tb, Gd, Eu and Cf, Bk, Cm, Am.
[2]
Weighable quantities of califorinium were first produced by long-duration irradiation of plutonium targets at the Materials Testing Reactor.[4] The high spontaneous fission rate of Cf-252 was observed in these samples.
In the 1960s, reactors at Savannah River and the High Flux Isotope Reactor(HFIR) started producing batches of californium regularly. The U.S. Atomic Energy Commission began selling and loaning californium sources to industrial and academic customers in 1970 for $10 per microgram. By the 1990s, Oak Ridge was producing 300-400 mg of Cf, mostly Cf-252, every two years.
Milligram-quantities of californium can only be made in specialized high-flux reactors; there are only two reactors operating that can efficiently produce it, the High Flux Isotope Reactor in the U.S. and Research Institute of Atomic Reactors in Dimitrovgrad, Russia, with HFIR filling about 2/3 of the world market of about 90 mg / year. Between 1960 and 1995, the HFIR produced only 8 grams of californium, peaking at about 200 mg per year.[5]
Plutonium supplied by the United Kingdom to the U.S. under the 1958 US-UK Mutual Defence Agreement was used for californium production.[6]
Isotopes
Twenty radioisotopes of californium have been characterized, the most stable being 251Cf with a half-life of 898 years, 249Cf with a half-life of 351 years, and 250Cf with a half-life of 13 years. All of the remaining radioactive isotopes have half-lives that are less than 2.7 years, and the majority of these have half-lives shorter than 20 minutes. The isotopes of californium range in atomic weight from 237.062 u (237Cf) to 256.093 u (256Cf).
Energy spectrum of neutrons emitted by
252Cf.
[7]
252Cf has a half life of 2.645 years. 252Cf undergoes α-decay 96.9% of the time while the remaining 3.1% of decays are spontaneous fission. Each spontaneous fission decay emits an average of 3.77 neutrons per fission. 254Cf decays nearly quantitatively by spontaneous fission with a half-life of 60.5 days. Both materials can be used as a neutron source.
Occurrence
Natural occurrence
Californium bromide CfBr
3
Although californium does not occur naturally on Earth, the element and its decay products occur elsewhere in the universe. Their electromagnetic emissions are regularly observed in the spectra of supernovae.[8][9][10][11]
Fallout
On November 1, 1952, the fallout of the United States hydrogen bomb test Ivy Mike contained plutonium, californium, einsteinium, and other transuranium elements. The isotopes 249Cf, 252Cf, 253Cf, and 254Cf were observed for the first time in the debris from the explosion.[12]
Characteristics
Weighable amounts of californium make it possible to determine some of its properties using macroscopic quantities.
252Cf (2.645-year half-life) is a very strong neutron emitter and is thus extremely radioactive and harmful.[13][14][15][16][17] One microgram spontaneously emits 2,314 million neutrons per second[18] and one gram emits 39 watts of heat[19]. 249Cf is formed from the beta decay of 249Bk and most other californium isotopes are made by subjecting berkelium to intense neutron radiation in a nuclear reactor.
Californium has no biological role and only a few californium compounds have been made and studied. Included among these are californium oxide (Cf2O3), californium trichloride (CfCl3) and californium oxychloride (CfOCl). The only californium ion that is stable in aqueous solution is the californium(III) cation.
Nuclear fuel cycle
Californium is produced by neutron capture on berkelium-249. Three californium isotopes with significant halflives are produced, requiring a total of 12 to 14 neutron captures on uranium-238 without nuclear fission or alpha decay. Their neutron cross sections are :
Thus 250Cf and 251Cf will be transmuted fairly quickly, with the majority fissioning at mass 251, but with a large fraction surviving to become 252Cf. The 252Cf will not be transmuted or destroyed quickly in a well-thermalized reactor, but has a short decay halflife. These isotopes decay into long-lived isotopes of curium.
252Cf has a relatively high rate of spontaneous fission. Although still much less likely than alpha decay, this makes californium a significant neutron radiation emitter. MOX fuel containing enough curium would likely contain enough californium after use to preclude manual handling of the spent fuel or its nuclear reprocessing products with a glove box that protects against alpha and beta radiation but not against gamma radiation and especially neutron radiation.
Applications
General
252Cf has a number of specialized applications as a strong neutron emitter. Each milligram of fresh californium produces 2.3 x 109 neutrons / second. Some of its uses are:[5][20][21]
In October 2006 it was announced that three atoms ununoctium (element 118) had been identified at the Joint Institute for Nuclear Research in Dubna as the product of bombardment of californium-249 with calcium-48 ,[24][25][26] making this the heaviest element ever synthesized.
Military
251Cf is famous for having a very small critical mass of 5 kg,[27] high lethality, and short period of toxic environmental irradiation relative to radioactive elements commonly used for radiation explosive weaponry, creating speculation about possible use in pocket nukes. Other weaponry uses, such as showering an area with californium, are not impossible but are seen as inhumane and are subject to inclement weather conditions and porous terrain considerations.
References
- ^ S. G. Thompson, K. Street, Jr., A. Ghiorso, G. T. Seaborg (1950). "Element 98". Physical Review 78: 298. doi:10.1103/PhysRev.78.298.2. http://repositories.cdlib.org/cgi/viewcontent.cgi?article=7072&context=lbnl.
- ^ a b c S. G. Thompson, K. Street, Jr., A. Ghiorso, G. T. Seaborg (1950). "The New Element Californium (Atomic Number 98)". Physical Review 80: 790. doi:10.1103/PhysRev.80.790. http://www.osti.gov/accomplishments/documents/fullText/ACC0050.pdf.
- ^ K. Street, Jr., S. G. Thompson, G. T. Seaborg (1950). "Chemical Properties of Californium". J. Am. Chem. Soc. 72: 4832. doi:10.1021/ja01166a528. http://handle.dtic.mil/100.2/ADA319899.
- ^ Diamond, H. (1954). "Identification of Californium Isotopes 249, 250, 251, and 252 from Pile-Irradiated Plutonium". Phys Rev 94 (4): 1083. doi:10.1103/PhysRev.94.1083.
- ^ a b Osborne-Lee, I.W. and Alexander, C. W. (1995). "Californium-252: A remarkable versatile radioisotope". Oak Ridge Technical Report ORNL/TM-12706. http://www.osti.gov/bridge/product.biblio.jsp?query_id=1&page=0&osti_id=205871.
- ^ "Plutonium and Aldermaston - an historical account". UK Ministry of Defence. 2001-09-04. http://www.mod.uk/NR/rdonlyres/B31B4EF0-A584-4CC6-9B14-B5E89E6848F8/0/plutoniumandaldermaston.pdf. Retrieved 2007-03-15.
- ^ K. Anderson, J. Pilcher, H. Wu, E. van der Bij, Z. Meggyesi, J. Adams (1999). "Neutron Irradiation Tests of an S-LINK-over-G-link System". http://hep.uchicago.edu/atlas/tilecal/rad/Glink_radtest.pdf.
- ^ G. R. Burbidge et al. (1956). "PDF Californium-254 and Supernovae". Physical Review 103: 1145. doi:10.1103/PhysRev.103.1145. http://authors.library.caltech.edu/6553/1/BURpr56.pdf PDF.
- ^ W. Baade, G. R. Burbidge, F. Hoyle, E. M. Burbidge, R. F. Christy, W. A. Fowler (1956). "Supernovae and Californium 254". Publications of the Astronomical Society of the Pacific 68: 296url = http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1956PASP...68..296B&link_type=ARTICLE&db_key=AST&high=14365.
- ^ St. Temesváry (1957). "Das Element Californium-254 und die Lichtkurven der Supernovae von Typ I. Ein Beitrag zur Frage der Synthese schwerer Elemente im Kosmos". Die Naturwissenschaften 44: 321. doi:10.1007/BF00630928. .
- ^ E. Anders (1959). "Californium-254, Iron-59, and Supernovae of Type I". The Astrophysical Journal 129: 327–346. doi:10.1086/146624. http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1959ApJ...129..327A&link_type=ARTICLE&db_key=AST&high=14365.
- ^ P. R. Fields et al. (1956). "Transplutonium Elements in Thermonuclear Test Debris". Physical Review 102 (1): 180–182. doi:10.1103/PhysRev.102.180.
- ^ D. A. Hicks et al. (1955). "Multiplicity of Neutrons from the Spontaneous Fission of Californium-252". Physical Review 97 (2): 564–565. doi:10.1103/PhysRev.97.564.
- ^ D. A. Hicks et al. (1955). "Spontaneous-Fission Neutrons of Californium-252 and Curium-244". Physical Review 98 (5): 1521–1523. doi:10.1103/PhysRev.98.1521.
- ^ E. Hjalmar, H. Slätis, S.G. Thompson (1955). "Energy Spectrum of Neutrons from Spontaneous Fission of Californium-252"". Physical Review 100 (5): 1542–1543. doi:10.1103/PhysRev.100.1542.
- ^ United States Patent 7118524: "Dosimetry for californium-252 (252Cf) neutron-emitting brachytherapy sources and encapsulation, storage, and clinical delivery thereof" bei www.freepatentsonline.com.
- ^ Michael B. Dillon, Ronald L. Baskett, Kevin T. Foster, and Connee S. Foster (2004-03-18). "The NARAC Emergency Response Guide to Initial Airborne Hazard Estimates". National Atmospheric Release Advisory Center. https://narac.llnl.gov/uploads/Dillon2004_NARACEmergencyResponseGuide_202990_xchnw.pdf. Retrieved 2008-11-14.
- ^ R. C. Martin, J. B. Knauer, P. A. Balo (2000, Pages 785–792). "PDF Production, Distribution, and Applications of Californium-252 Neutron Sources". Applied Radiation and Isotopes 53. doi:10.1016/S0969-8043(00)00214-1. http://www.osti.gov/bridge/servlets/purl/15053-AE6cnN/native/15053.pdf PDF.
- ^ http://www.britannica.com/EBchecked/topic/603220/transuranium-element/81185/Nuclear-properties
- ^ R. C. Martin and J. H. Miller. "Applications of Californium-252 Neutron Sources in Medicine, Research, and Industry" (PDF). http://anes.fiu.edu/Pro/s7Mar.pdf. Retrieved 2008-11-14.
- ^ R. C. Martin (2000). "Applications and Availability of Californium-252 Neutron Sources for Waste Characterization" (PDF). http://www.ornl.gov/~webworks/cpr/pres/107270_.pdf. Retrieved 2009-05-05.
- ^ "Will you be 'mine'? Physics key to detection". Pacific Northwest National Laboratory. 2000-10-25. http://www.pnl.gov/news/2000/00-43.htm. Retrieved 2007-03-21.
- ^ S. N. Davis et al. (2006). "Ground-Water Tracers — A Short Review". Ground Water 18 (1): 14–23. doi:10.1111/j.1745-6584.1980.tb03366.x.
- ^ Yu. Ts. Oganessian et al. (2006). "Synthesis of the isotopes of elements 118 and 116 in the 249Cf and 245Cm+48Ca fusion reactions". Physical Review C 74: 044602–044611. doi:10.1103/PhysRevC.74.044602. .
- ^ K. Sanderson (2006-10-17). "Heaviest element made - again". nature@news.com (Nature). http://www.nature.com/news/2006/061016/full/061016-4.html. Retrieved 2006-10-19.
- ^ Phil Schewe and Ben Stein (2006-10-17). "Elements 116 and 118 Are Discovered". Physics News Update. American Institute of Physics. http://www.aip.org/pnu/2006/797.html. Retrieved 2006-10-19.
- ^ "Evaluation of nuclear criticality safety data and limits for actinides in transport" (PDF). Institut de Radioprotection et de Sûreté Nucléaire. p. 16. http://ec.europa.eu/energy/nuclear/transport/doc/irsn_sect03_146.pdf.
Literature
- Guide to the Elements - Revised Edition, Albert Stwertka, (Oxford University Press; 1998) ISBN 0-19-508083-1
External links