'Francium' (
IPA: ), formerly known as '
eka-
caesium' and 'actinium K',
[1] is a
chemical element that has the symbol 'Fr' and
atomic number 87. It has the lowest known
electronegativity and is the
second rarest naturally occurring element (after
Astatine). Francium is a highly
radioactive metal that decays into
astatine,
radium, and
radon. As an
alkali metal, it has one
valence electron.
Marguerite Perey discovered francium in 1939. Francium was the last element discovered in
nature, rather than synthesized.
[2] Outside the laboratory, francium is extremely rare, with trace amounts found in
uranium and
thorium ores, where the
isotope francium-223 is continually formed and continually decays. Perhaps an ounce exists at any given time throughout the
Earth's
crust; the other isotopes are entirely synthetic. The largest amount ever collected of any isotope was a cluster of 10,000 atoms (of francium-210) created as an ultracold gas at Stony Brook in 1996.
[3]
Characteristics
Francium is less stable than any other element lighter than
nobelium, element 102;
3 its most stable isotope, francium-223, has a
half-life of less than 22 minutes. By contrast,
astatine, the next least stable element, has a maximum half-life of 8.5 hours.
4 All isotopes of francium decay into either astatine,
radium, or
radon.
[4]
Francium is an
alkali metal whose chemical properties most resemble those of
caesium.
3 As a very heavy element with a single
valence electron;
[5] it therefore has the highest
equivalent weight of any element.
3 Similarly, Francium has the lowest
electronegativity of all the known elements at 0.7 on the
Pauling scale;
[6] caesium has the second-lowest at 0.79.
[7] Liquid francium, if such a substance were created, should have a surface tension of 0.05092
J/
m² at its melting point.
[8]
Francium
coprecipitates with several caesium
salts, such as
caesium perchlorate, which results in small amounts of francium perchlorate. This coprecipitation can be used to isolate francium, by adapting the radiocaesium coprecipitation method of Glendenin and Nelson. It will also coprecipitate with many other caesium salts, including the
iodate, the
picrate, the
tartrate (also
rubidium tartrate), the
chloroplatinate, and the
silicotungstate. It also coprecipitates with
silicotungstic acid, and with
perchloric acid, without another alkali metal as a
carrier, which provides other methods of separation.
[9][10] Nearly all francium salts are
water-soluble.
[11]
Applications
There are no commercial applications for francium due to its instability and rarity;
[12][13][14][15]32 it has only been used for research purposes, both in the fields of
biology and
atomic structure. Francium was once thought to be an aid in the diagnosis of cancerous diseases;
4 but, this application has since been deemed impracticable.
14
Francium's ability to be synthesized, trapped, and cooled, along with its relatively simple
atomic structure have made it the subject of specialized
spectroscopy experiments. These experiments have led to more specific information regarding
energy levels and the coupling constants between
subatomic particles.
[16] Studies on the light emitted by laser-trapped francium-210 ions have provided accurate data on transitions between atomic energy levels. These experimental results have been fairly similar to those predicted by
quantum theory.
[17]
History
As early as 1870, it was thought by chemists that there should be an alkali metal beyond caesium, with an atomic number of 87.
4 It was then referred to by the provisional name ''
eka-caesium.''
[18] Research teams attempted to locate and isolate this missing element, and at least four false claims were made that the element had been found before an authentic discovery was made.
Erroneous and incomplete discoveries
Russian chemist D. K. Dobroserdov was the first scientist to claim to have found "eka-caesium". In 1925, he observed weak
radioactivity in a sample of
potassium, another alkali metal, and concluded that eka-caesium was contaminating the sample.
[19] He then published a thesis of his predictions of the properties of eka-caesium, in which he named the element ''russium'' after his home country.
[20] Shortly thereafter, Dobroserdov began to focus on his teaching career at the Polytechnic Institute of Odessa, and he did not pursue the element further.
The
following year,
English chemists Gerald J. F. Druce and Frederick H. Loring analyzed
X-ray photographs of
manganese(II) sulfate.
They observed spectral lines which they presumed to be of eka-caesium. They announced their discovery of element 87 and proposed the name ''alkalinium'', as it would be the heaviest alkali metal.
In 1930, Professor Fred Allison of the
Alabama Polytechnic Institute claimed to have discovered element 87 when analyzing
pollucite and
lepidolite using his
magneto-optical machine. Allison requested that it be named ''virginium'' after his home state of
Virginia, along with the symbols ''Vi'' and ''Vm''.
[21] In 1934, however, Professor MacPherson of
UC Berkeley disproved the effectiveness of Allison's device and the validity of this false discovery.
[22]
In 1936,
Romanian chemist Horia Hulubei and his
French colleague Yvette Cauchois also analyzed pollucite, this time using their high-resolution X-ray apparatus.
They observed several weak emission lines which they presumed to be of element 87. Hulubei and Cauchois reported their discovery and proposed the name ''moldavium'', along with the symbol ''Ml'', after
Moldavia, the Romanian province where they conducted their work.
In 1937, Hulubei's work was criticized by American physicist F. H. Hirsh Jr., who rejected Hulubei's research methods. Hirsh was certain that eka-caesium would not be found in nature, and that Hulubei had instead observed
mercury or
bismuth X-ray lines. Hulubei, however, insisted that his X-ray apparatus and methods were too accurate to make such a mistake. Because of this,
Jean Baptiste Perrin,
Nobel Prize winner and Hulubei's mentor, endorsed moldavium as the true eka-caesium over
Marguerite Perey's recently-discovered francium. Perey, however, continuously criticized Hulubei's work until she was credited as the sole discoverer of element 87.
Perey's analysis
Eka-caesium was truly discovered in 1939 by
Marguerite Perey of the Curie Institute in
Paris,
France, when she purified a sample of
actinium-227 which had been reported to have a decay energy of 220 keV. However, Perey noticed decay particles with an energy level below 80 keV. Perey thought this decay activity might have been caused by a previously unidentified decay product, one which was separated during purification, but emerged again out of the pure actinium-227. Various tests eliminated the possibility of
thorium,
radium,
lead,
bismuth, or
thallium being the unknown element. The new product exhibited chemical properties of an alkali metal (such as co-precipitating with caesium salts), which led Perey to believe that it was element 87, caused by the
alpha decay of actinium-227.
18 Perey then attempted to determine the proportion of beta decay to alpha decay in actinium-227. Her first test put the alpha branching at .6%, which she later revised to 1%.
28
Perey named the new isotope ''actinium-K'', which we now refer to as francium-223,
18 and in 1946, she proposed the name ''catium'' for her newly-discovered element, as she believed it to be the most
electropositive cation of the elements.
Irène Joliot-Curie, one of Perey's supervisors, opposed the name due to its connotation of ''cat'' rather than ''cation''.
Perey then suggested ''francium'' as an homage to the country in which she discovered it. This name was officially adopted by the International Union of Chemists in 1949.
4 and assigned the symbol ''Fa''; but, this abbreviation was revised to the current ''Fr'' shortly thereafter.
[23] Francium was the last naturally occurring element to be discovered, following
rhenium in 1925.
18 Further research into francium's structure was carried out by
Sylvain Lieberman and his team at
CERN in the 1970s and 1980s, among others.
[24]
Occurrence
Natural
Francium-223 is the result of the
alpha decay of actinium-227 and can be found in trace amounts in
uranium and
thorium minerals.
[25] This makes it the second
rarest element in the crust after
astatine.
414
Synthesized
Francium can be synthesized in the nuclear reaction
197Au +
18O →
210Fr + 5n. This process, developed by
Stony Brook Physics, yields francium isotopes with masses of 209, 210, and 211,
[26] which are then isolated by the
Magneto Optic Trap (MOT).
[27] Other synthesis methods include bombarding radium with neutrons, and bombarding thorium with protons,
deuterons, or
helium ions.
[28] Francium has not yet,
as of 2006, been synthesized in amounts large enough to weigh.
3414[29]
Isotopes
Main articles: Isotopes of francium
There are 34 known isotopes of francium ranging in
atomic mass from 199 to 232.
[3] Francium has seven metastable
nuclear isomers.
3 Francium-223 and francium-221 are the only isotopes that occur in nature, though the former is far more common.
[31]
Francium-223 is the most stable isotope with a
half-life of 21.8 minutes,
3 and it is highly unlikely that an isotope of francium will ever be discovered or synthesized with one longer.
28 Francium-223 is the fifth product of the
actinium decay series as the daughter isotope of actinium-227.
[32] Francium-223 then decays into
radium-223 by
beta decay (1149 keV
decay energy), with a minor (0.006%)
alpha decay path to
astatine-219 (5.4 MeV decay energy).
[33]
Francium-221 has a half-life of 4.8 minutes.
3 It is the ninth product of the
neptunium decay series as a daughter isotope of actinium-225.
32 Francium-221 then decays into astatine-217 by alpha decay (6.457 MeV decay energy).
3
The least stable
ground state isotope is francium-215, with a half-life of 0.12 μs. (9.54 MeV alpha decay to astatine-211):
3 Its metastable isomer, francium-215m, is less stable still, with a half-life of only 3.5 ns.
[34]
See Also
References
1. Actually the least unstable isotope, Fr-223
2. Some synthetic elements, like technetium, have later been found in nature.
3.
4. Francium
5. Electron Configuration
6. The Nature of the Chemical Bond (3rd Edn.), , Linus, Pauling, Cornell University Press, 1960,
7. Electronegativies Pauling places caesium and francium with the same electronegativity.
8. Evaluation of the Surface Tension of Liquid Francium, , L. V., Kozhitov, Inorganic Materials,
9. E. K. Hyde. Radiochemical Methods for the Isolation of Element 87 (Francium). ''J. Am. Chem. Soc.'' '1952', ''74'', 4181-4184.[1].
10. E. N K. Hyde ''Radiochemistry of Francium'',Subcommittee on Radiochemistry, National Academy of Sciences-National Research Council; available from the Office of Technical Services, Dept. of Commerce, 1960.
11. A. G. Maddock. Radioactivity of the heavy elements. ''Q. Rev., Chem. Soc.'', '1951', ''3'', 270–314.
12. Uses
13. Chemical Element.com - Francium
14. Nature's Building Blocks, , John, Emsley, Oxford University Press, , 0-19-850341-5
15. Francium
16. Spectroscopy with trapped francium: advances and perspectives for weak interaction studies, , E, Gomez, Rep. Prog. Phys.,
17. Creating, cooling, trapping francium atoms I Peterson
18. Adloff, Jean-Pierre; Kaufman, George B. (2005-09-25). Francium (Atomic Number 87), the Last Discovered Natural Element. ''The Chemical Educator'' '10' (5). Retrieved on 2007-03-26.
19.
20. Francium
21. Alabamine & Virginium
22. An Investigation of the Magneto-Optic Method of Chemical Analysis, , H. G., MacPherson, Physical Review,
23.
24. History
25. In a given sample of uranium, there is estimated to be only one francium atom for every 1×1018 uranium atoms. It is also calculated that there is at most 30 g of francium in the earth's crust at any time.[ Geological information ]
26. Production of Francium
27. Cooling and Trapping
28.
29. Francium
30.
31.
32.
33. Table of Isotopes decay data National Nuclear Data Center .
34. Fr Isotopes National Nuclear Data Center .
External links
★
WebElements.com - Francium
★
Los Alamos National Laboratory - Francium
★
Stony Brook University Physics Dept.