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promethium

 
Dictionary: pro·me·thi·um   (prə-mē'thē-əm) pronunciation
n. (Symbol Pm)
A radioactive rare-earth element prepared by fission of uranium or by neutron bombardment of neodymium, having 14 isotopes with mass numbers ranging from 141 to 154 and used as a source of beta rays. Atomic number 61; melting point 1,168°C; boiling point 2,460°C; valence 3.

[From PROMETHEUS.]


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Sci-Tech Encyclopedia: Promethium
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A chemical element, Pm, atomic number 61. Promethium is the “missing” element of the lanthanide rare-earth series. The atomic weight of the most abundant separated radioisotope is 147. See also Periodic table.

Although a number of scientists have claimed to have discovered this element in nature as a result of observing certain spectral lines, no one has succeeded in isolating element 61 from naturally occurring materials. It is produced artificially in nuclear reactors, since it is one of the products that results from the fission of uranium, thorium, and plutonium.

All the known isotopes are radioactive. Its principal uses are for research involving tracers. Its main application is in the phosphor industry. It has also been used to manufacture thickness gages and as a nuclear-powered battery in space applications. See also Rare-earth elements.


 
Columbia Encyclopedia: promethium
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promethium (prōmē'thēəm), artificially produced radioactive chemical element; symbol Pm; at. no. 61; mass no. of most stable isotope 145; m.p. 1,042°C; b.p. 3,000°C (estimated); sp. gr. unknown; valence +3. Although the chemical and physical properties of promethium are not well defined, it is similar to neodymium and samarium, the rare-earth metals preceding and following it in the lanthanide series in Group 3 of the periodic table. All its isotopes are radioactive and fairly short-lived. Promethium-145, the most stable isotope, has a half-life of almost 18 years. The most useful isotope is promethium-147 (half-life 2.64 years); it is produced in nuclear reactors. It is a beta emitter and is used in making phosphorescent materials. When it is mixed with a phosphor, the light emitted can be used to power a photocell. It must be used with caution; although the beta rays it emits are relatively harmless, they may produce X rays when they interact with atoms of heavy elements. The existence of promethium was predicted at the beginning of the 20th cent. In 1926, B. S. Hopkins and his coworkers claimed to have discovered the element and proposed the name illinium. About the same time Luigi Rolla and his associates (in Italy) reported its discovery and suggested the name florentium. However, definite chemical identification of the element did not occur until 1947, although it may have been synthesized earlier. J. A. Marinsky, L. E. Glendenin, and C. D. Coryell identified the element by ion-exchange chromatography during the course of experiments at Oak Ridge National Laboratory, Tenn., involving the fission of uranium and subsequent neutron bombardment of neodymium. Since observable quantities of the element have never been found in nature, this identification is considered the first actual discovery of the element. The name promethium was suggested by these investigators and adopted in 1949 by the International Union of Pure and Applied Chemistry.


Veterinary Dictionary: promethium
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A chemical element, atomic number 61, atomic weight 147, symbol Pm.

Wikipedia: Promethium
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neodymiumpromethiumsamarium
-

Pm

Np
Appearance
metallic
General properties
Name, symbol, number promethium, Pm, 61
Element category lanthanide
Group, period, block n/a6, f
Standard atomic weight [145]g·mol−1
Electron configuration [Xe] 4f5 6s2
Electrons per shell 2, 8, 18, 23, 8, 2 (Image)
Physical properties
Phase solid
Density (near r.t.) 7.26 g·cm−3
Melting point 1315 K, 1042 °C, 1908 °F
Boiling point 3273 K, 3000 °C, 5432 °F
Heat of fusion 7.13 kJ·mol−1
Heat of vaporization 289 kJ·mol−1
Atomic properties
Oxidation states 3 (mildly basic oxide)
Electronegativity  ? 1.13 (Pauling scale)
Ionization energies 1st: 540 kJ·mol−1
2nd: 1050 kJ·mol−1
3rd: 2150 kJ·mol−1
Atomic radius 183 pm
Covalent radius 199 pm
Miscellanea
Crystal structure hexagonal
Magnetic ordering paramagnetic[1]
Electrical resistivity (r.t.) est. 0.75 µΩ·m
Thermal conductivity (300 K) 17.9 W·m−1·K−1
Thermal expansion (r.t.) (α, poly)
est. 11 µm/(m·K)
Young's modulus (α form) est. 46 GPa
Shear modulus (α form) est. 18 GPa
Bulk modulus (α form) est. 33 GPa
Poisson ratio (α form) est. 0.28
CAS registry number 7440-12-2
Most stable isotopes
Main article: Isotopes of promethium
iso NA half-life DM DE (MeV) DP
145Pm syn 17.7 y ε 0.163 145Nd
146Pm syn 5.53 y ε 1.472 146Nd
β 1.542 146Sm
147Pm trace 2.6234 y β 0.224 147Sm

Promethium (pronounced /prɵˈmiːθiəm/, pro-MEE-thee-əm) is a chemical element with the symbol Pm and atomic number 61. It is notable for being the only other exclusively radioactive element besides technetium which is followed by chemical elements that have stable isotopes.

Contents

Characteristics

Physical

Promethium's longest lived isotope 145Pm is a soft beta emitter with a half-life of 17.7 years. It does not emit gamma rays, but beta particles impinging on elements of high atomic numbers can generate X-rays, and a sample of 145Pm does produce some such soft X-ray radiation in addition to beta particles.

Pure promethium exists in two allotropic forms, and its chemistry is similar to other lanthanides. Promethium salts luminesce in the dark with a pale blue or greenish glow, due to their high radioactivity. Promethium can be found in traces in some uranium ores, as a fission product. Newly made promethium is also seen in the spectra of some stars.

Chemical

Promethium metal tarnishes slowly in air and burns readily at 150 °C to form promethium(III) oxide:

4 Pm + 3 O2 → 2 Pm2O3

Promethium is quite electropositive and reacts slowly with cold water and quite quickly with hot water to form promethium hydroxide:

2 Pm (s) + 6 H2O (l) → 2 Pm(OH)3 (aq) + 3 H2 (g)

Promethium metal reacts with all the halogens:

2 Pm (s) + 3 F2 (g) → 2 PmF3 (s)
2 Pm (s) + 3 Cl2 (g) → 2 PmCl3 (s)
2 Pm (s) + 3 Br2 (g) → 2 PmBr3 (s)
2 Pm (s) + 3 I2 (g) → 2 PmI3 (s)

Promethium dissolves readily in dilute sulfuric acid to form solutions containing the pink Pm(III) ions, which exist as a [Pm(OH2)9]3+ complexes:[2]

2 Pm(s) + 3 H2SO4 (aq) → 2 Pm3+ (aq) + 3 SO2−4 (aq) + 3 H2 (g)

Compounds

Promethium compounds include:

  • Chlorides
    • PmCl3
  • Bromides
    • PmBr3
  • Oxides

Isotopes

Thirty-six radioisotopes of promethium have been characterized, with the most stable being 145Pm with a half-life of 17.7 years, 146Pm with a half-life of 5.53 years, and 147Pm with a half-life of 2.6234 years. All of the remaining radioactive isotopes have half-lives that are less than 364 days, and the majority of these have half lives that are less than 27 seconds. This element also has 11 meta states with the most stable being 148Pmm (T½ 41.29 days), 152Pmm2 (T½ 13.8 minutes) and 152Pmm (T½ 7.52 minutes).

The isotopes of promethium range in atomic weight from 127.9482600 u (128Pm) to 162.9535200 u (163Pm). The primary decay mode before the longest-lived isotope, 145Pm, is electron capture, and the primary mode after is beta minus decay. The primary decay products before 145Pm are neodymium (Nd) isotopes and the primary products after are samarium (Sm) isotopes.

Along with technetium, promethium is one of only two elements with atomic number less than 83 that have only unstable isotopes, which is a rarely occurring effect of the liquid drop model and stabilities of neighbor element isotopes.

History

The existence of promethium was first predicted by Bohuslav Brauner in 1902. During his research on the chemical properties of rare earth elements he found that the difference between neodymium and samarium is larger than between the other lanthanoids. This prediction was supported in 1914 by Henry Moseley who, having discovered that atomic number was an experimentally measurable property of elements, found that no known element had atomic number 61. With the knowledge of a gap in the periodic table several groups started to search for the new element in natural environment.

The first discovery was published by Italian scientists Luigi Rolla and Lorenzo Fernandes from Florence. After separating a didymium nitrate concentrate from the Brazilian mineral monazite, which contained 70% dysprosyium and neodymium with the other lantanoides making up the additional 30%, by fractionated crystalisation, they yielded a solution containing mostly samarium. This solution gave x-ray spectra atributed to samarium and element 61. In honor of their city they named element 61 Florentium. The results were published in 1926, but the scientists claimed that the experiments were done in 1924.[3][4] [5][6][7][8] In the same year 1926 a group of scientists University of Illinois at Urbana-Champaign Smith Hopkins and Len Yntema published the discovery of element 61. They named it after the university illinium.[9][10][11] Neither of the two discoveries could be verified.

So several groups claimed to have produced the element, but they could not confirm their discoveries because of the difficulty of separating promethium from other elements. Promethium was first produced and proved to exist at Oak Ridge National Laboratory (ORNL) in 1945 by Jacob A. Marinsky, Lawrence E. Glendenin and Charles D. Coryell by separation and analysis of the fission products of uranium fuel irradiated in the Graphite Reactor; however, being too busy with defense-related research during World War II, they did not announce their discovery until 1947.[12] The name promethium is derived from Prometheus, the Titan, in Greek mythology, who stole the fire from Mount Olympus and brought it down to mankind. The name was suggested by Grace Mary Coryell, Charles Coryell's wife, who felt that they were stealing fire from the gods.

In 1963, ion-exchange methods were used at ORNL to prepare about ten grams of promethium from nuclear reactor fuel processing wastes.[13][14]

Today, promethium is still recovered from the byproducts of uranium fission; it can also be produced by bombarding 146Nd with neutrons, turning it into 147Nd which decays into 147Pm through beta decay with a half-life of 11 days.

Occurrence

Pitchblende

Promethium can be formed in nature as a product of spontaneous fission of uranium-238 and alpha decay of europium-151. Only trace amounts can be found in naturally occurring ores: a sample of pitchblende has been found to contain promethium at a concentration of four parts per quintillion (1018) by mass.[15] It was calculated that the equilibrium mass of promethium in the earth's crust is about 560 g due to uranium fission and about 12 g due to the recently observed alpha decay of europium-151.[16]

Promethium has also been identified in the spectrum of the star HR 465 in Andromeda, and possibly HD 101065 (Przybylski's star) and HD 965.[17]

Applications

Uses for promethium include:

  • As a beta radiation source for thickness gauges.
  • As a light source for signals that require reliable, independent operation (using phosphor to absorb the beta radiation and produce light).
  • In a nuclear battery in which cells convert the beta emissions into electric current, yielding a useful life of about five years, using Pm-147.
  • Promethium(III) chloride (PmCl3) mixed with zinc sulfide (ZnS) was used for a time as a major luminous paint for watches after radium was discontinued. This mixture is still occasionally used for some luminous paint applications (though most such uses with radioactive materials have switched to tritium for safety reasons).
  • Promethium has possible future uses in portable X-ray sources, and as auxiliary heat or power sources for space probes and satellites (although the alpha emitter plutonium-238 has become standard for most space-exploration related uses – see Radioisotope thermoelectric generators).

Precautions

Promethium must be handled with great care because of its high radioactivity. In particular, promethium can emit X-rays during its beta decay. Its half-life is less than that of plutonium-239 by a factor of about 1350, and its biological toxicity is correspondingly higher. Promethium has no biological role.

References

  1. ^ Magnetic susceptibility of the elements and inorganic compounds, in Handbook of Chemistry and Physics 81th edition, CRC press.
  2. ^ "Chemical reactions of Promethium". Webelements. https://www.webelements.com/promethium/chemistry.html. Retrieved 2009-06-06. 
  3. ^ . doi:10.1002/zaac.19261570129. 
  4. ^ Noyes, W. A. (1927). "Florentium or Illinium?". Nature 120: 14. doi:10.1038/120014c0. 
  5. ^ Rolla, L. (1927). "Florentium or Illinium?". Nature 119: 637. doi:10.1038/119637a0. 
  6. ^ Rolla, Luigi (1928). "Florentium. II". Zeitschrift für anorganische und allgemeine Chemie 169: 319. doi:10.1002/zaac.19281690128. 
  7. ^ Rolla, Luigi (1927). "Florentium". Zeitschrift für anorganische und allgemeine Chemie 163: 40. doi:10.1002/zaac.19271630104. 
  8. ^ Rolla, Luigi (1927). "Über Das Element der Atomnummer 61 (Florentium)". Zeitschrift für anorganische und allgemeine Chemie 160: 190. doi:10.1002/zaac.19271600119. 
  9. ^ Harris, J. A. (1926). "The Element of Atomic Number 61; Illinium". Nature 117: 792. doi:10.1038/117792a0. 
  10. ^ Brauner, BOHUSLAV (1926). "The New Element of Atomic Number 61: Illinium". Nature 118: 84. doi:10.1038/118084b0. 
  11. ^ Meyer, R. J. (1926). "Über das Element 61 (Illinium)". Naturwissenschaften 14: 771. doi:10.1007/BF01490264. 
  12. ^ "Discovery of Promethium". ORNL Review 36 (1). 2003. http://www.ornl.gov/info/ornlreview/v36_1_03/article_02.shtml. Retrieved 2006-09-17. 
  13. ^ Lee, Chung-Sin (1989). "Chemical study on the separation and purification of promethium-147". Journal of Radioanalytical and Nuclear Chemistry Articles 130: 21. doi:10.1007/BF02037697. 
  14. ^ "ION EXCHANGE PURIFICATION OF PROMETHIUM-147 AND ITS SEPARATION FROM AMERICIUM-241, WITH DIETHYLENETRIAMINEPENTA-ACETIC ACID AS THE ELUANT". http://www.ornl.gov/info/reports/1962/3445605484259.pdf. 
  15. ^ Attrep, Moses, Jr.; and P. K. Kuroda (May 1968). "Promethium in pitchblende". Journal of Inorganic and Nuclear Chemistry 30 (3): 699–703. doi:10.1016/0022-1902(68)80427-0. 
  16. ^ P. Belli, R. Bernabei, F. Cappella, R. Cerulli, C.J. Dai, F.A. Danevich, A. d’Angelo, A. Incicchitti, V.V. Kobychev, S.S. Nagorny, S. Nisi, F. Nozzoli, D. Prosperi, V.I. Tretyak, S.S. Yurchenko (2007). "Search for α decay of natural Europium". Nuclear Physics A 789: 15–29. doi:10.1016/j.nuclphysa.2007.03.001. 
  17. ^ C. R. Cowley, W. P. Bidelman, S. Hubrig, G. Mathys, and D. J. Bord (2004). "On the possible presence of promethium in the spectra of HD 101065 (Przybylski's star) and HD 965". Astronomy & Astrophysics 419: 1087–1093. doi:10.1051/0004-6361:20035726. 

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