Template:About Template:Use mdy dates Template:Featured article 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.

CharacteristicsEdit

Physical propertiesEdit

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 compoundsEdit

Template:Further

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.<ref>Template:Cite journal</ref>

IsotopesEdit

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} Twenty isotopes of californium are known (mass number ranging from 237 to 256<ref name="NNDC2008" />); 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.<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" />

249Cf 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.Template:Sfn 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).Template:Sfn

252Cf is a very strong neutron emitter, which makes it extremely radioactive and harmful.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> 252Cf, 96.9% of the time, alpha decays to curium-248; the other 3.1% of decays are spontaneous fission.<ref name="NNDC2008" /> One microgram (μg) of 252Cf emits 2.3 million neutrons per second, an average of 3.7 neutrons per spontaneous fission.<ref name="osti">Template:Cite journal</ref> Most other isotopes of californium, alpha decay to curium (atomic number 96).<ref name="NNDC2008" />

HistoryEdit

File:Berkeley 60-inch cyclotron.jpg
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.<ref name="CPoC1950">Template:Cite journal</ref><ref>Template:Cite book</ref>

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<ref name="CPoC1950" />

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

To identify and separate out the element, ion exchange and adsorsion methods were undertaken.<ref name="CPoC1950" /><ref>Template:Cite journal</ref> 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.<ref>Template:Cite journal</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.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.<ref>Template:Cite journal</ref>

The High Flux Isotope Reactor (HFIR) at ORNL in Oak Ridge, Tennessee, started producing small batches of californium in the 1960s.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> 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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

The Atomic Energy Commission sold 252Cf to industrial and academic customers in the early 1970s for $10/microgram,<ref name="osti" /> 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<ref>Template:Cite journal</ref>Template:Efn

OccurrenceEdit

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.<ref name="ANL2005">{{#invoke:citation/CS1|citation |CitationClass=web }}</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>Template:Cite journal</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 supernovas, as their decay matches the 60-day half-life of 254Cf.<ref name="super1">Template:Cite journal</ref> However, subsequent studies failed to demonstrate any californium spectra,<ref name="super2">Template:Cite journal</ref> and supernova light curves are now thought to follow the decay of nickel-56.Template:Sfn

The transuranic elements americium to fermium, including californium, occurred naturally in the natural nuclear fission reactor at Oklo, but no longer do so.<ref name="emsley">Template:Cite book</ref>

Spectral lines of californium, along with those of several other non-primordial elements, were detected in Przybylski's Star in 2008.<ref name=gopka08>Template:Cite journal</ref>

ProductionEdit

Template:See also 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).

File:Cf 252 Produktion.png
Scheme of the production of californium-252 from uranium-238 by neutron irradiation

ApplicationsEdit

File:CfShield.JPG
CitationClass=web }}</ref>

Neutron source

Template:SimpleNuclide has a number of specialized uses as a strong neutron emitter; it produces 139 million neutrons per microgram per minute.<ref name="osti" /> 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.<ref name="Martin2000">Template:Cite conference</ref>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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> 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.<ref>Template:Cite journal</ref> 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.<ref>Template:Cite journal</ref>

Superheavy element productionEdit

Template:See also 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.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> 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>Template:Cite journal</ref>

Hypothetical nuclear weaponsEdit

Template:See also Template:SimpleNuclide has a very small calculated critical mass of about Template:Convert,<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</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.Template:Efn

PrecautionsEdit

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.<ref name="ANL2005" />

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.<ref name="ANL2005" />

NotesEdit

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ReferencesEdit

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BibliographyEdit

External linksEdit

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