61
Pm
Promethium
Atomic Mass 145
Electron Configuration [Xe]6s24f5
Oxidation States +3
Year Discovered 1945

Identifiers

Element Name Promethium
Element Symbol Pm
InChI InChI=1S/Pm
InChIKey VQMWBBYLQSCNPO-UHFFFAOYSA-N

Properties

Atomic Weight

145

145

[145]

Electron Configuration

[Xe]6s24f5

Atomic Radius

Van der Waals Atomic Radius : 236 pm (Van der Waals)

Empirical Atomic Radius : 185pm (Empirical)

Covalent Atomic Radius : 199 pm (Covalent)

Oxidation States

+3

3, 2 ​(a mildly basic oxide)

Ground Level

65/2

Ionization Energy

5.55 eV

5.58187 ± 0.00004 eV

Atomic Spectra

Lines Holdings

Levels Holdings

Physical Description

Solid

Element Classification

Metal

Element Period Number

6

Element Group Number

- Lanthanide

Density

7.26 grams per cubic centimeter

Melting Point

1315 K (1042°C or 1908°F)

1042°C

Boiling Point

3273 K (3000°C or 5432°F)

3000°C

Estimated Crustal Abundance

Not Applicable

Estimated Oceanic Abundance

Not Applicable

History

The existence of promethium was predicted by Bohuslav Brauner, a Czech chemist, in 1902. 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. Proof of the existence of promethium was obtained by Jacob A. Marinsky, Lawrence E. Glendenin and Charles D. Coryell in 1944. Too busy with defense related research in World War II, they did not claim their discovery until 1946. They discovered promethium while analyzing the byproducts of uranium fission that were produced in a nuclear reactor located at Clinton Laboratories in Oak Ridge, Tennessee. Today, Clinton Laboratories is known as Oak Ridge National Laboratory. Today, promethium is still recovered from the byproducts of uranium fission. It can also be produced by bombarding neodymium-146 with neutrons. Neodymium-146 becomes neodymium-147 when it captures a neutron. Neodymium-147, with a half-life of 11 days, decays into promethium-147 through beta decay. Promethium does not occur naturally on earth, although it has been detected in the spectrum of a star in the constellation Andromeda.

Promethium's most stable isotope, promethium-145, has a half-life of 17.7 years. It decays into neodymium-145 through electron capture.

Named after the Greek Prometheus, who, according to mythology, stole fire from heaven. In 1902 Branner predicted the existence of an element between neodymium and samarium, and this was confirmed by Moseley in 1914. In 1941, workers at Ohio State University irradiated neodymium and praseodymium with neutrons, deuterons, and alpha particles, and produced several new radioactivities, which most likely were those of element 61. Wu and Segre, and Bethe, in 1942, confirmed the formation; however, chemical proof of the production of element 61 was lacking because of the difficulty in separating the rare earths from each other at that time. In 1945, Marinsky, Glendenin, and Coryell made the first chemical identification by use of ion-exchange chromatography. Their work was done by fission of uranium and by neutron bombardment of neodymium.

Description

It is a soft beta emitter; although no gamma rays are emitted, X-radiation can be generated when beta particles impinge on elements of a high atomic number, and great care must be taken in handling it. Promethium salts luminesce in the dark with a pale blue or greenish glow, due to their high radioactivity. Ion-exchange methods led to the preparation of about 10 g of promethium from atomic reactor fuel processing wastes in early 1963. Little is yet generally known about the properties of metallic promethium. Two allotropic modifications exist.

Users

Promethium could be used to make a nuclear powered battery. This type of battery would use the beta particles emitted by the decay of promethium to make a phosphor give off light. This light would then be converted into electricity by a device similar to a solar cell. It is expected that this type of battery could provide power for five years.

Promethium could also be used as a portable X-ray source, in radioisotope thermoelectric generators to provide electricity for space probes and satellites, as a source of radioactivity for gauges that measure thickness and to make lasers that can be used to communicate with submerged submarines.

The element has applications as a beta source for thickness gages, and it can be absorbed by a phosphor to produce light. Light produced in this manner can be used for signs or signals that require dependable operation; it can be used as a nuclear-powered battery by capturing light in photocells which convert it into electric current. Such a battery, using 147Pm, would have a useful life of about 5 years. Promethium shows promise as a portable X-ray source, and it may become useful as a heat source to provide auxiliary power for space probes and satellites. More than 30 promethium compounds have been prepared. Most are colored.

Sources

Searches for the element on earth have been fruitless, and it now appears that promethium is completely missing from the earth's crust. Promethium, however, has been identified in the spectrum of the star HR465 in Andromeda. This element is being formed recently near the star's surface, for no known isotope of promethium has a half-life longer than 17.7 years. Seventeen isotopes of promethium, with atomic masses from 134 to 155 are now known. Promethium-147, with a half-life of 2.6 years, is the most generally useful. Promethium-145 is the longest lived, and has a specific activity of 940 Ci/g.

Compounds

See more information at the Promethium compound page.

Element Forms

CID Name Formula SMILES Molecular Weight
23944 promethium Pm [Pm] 144.91276
104906 promethium-147 Pm [147Pm] 146.91514
161149 promethium-149 Pm [149Pm] 148.91834
167342 promethium-145 Pm [145Pm] 144.91276
177521 promethium-141 Pm [141Pm] 140.9136
177645 promethium-150 Pm [150Pm] 149.9210
167138 promethium-148 Pm [148Pm] 147.91748
167177 promethium-143 Pm [143Pm] 142.91094
177486 promethium-146 Pm [146Pm] 145.91470
177485 promethium-144 Pm [144Pm] 143.91260
177678 promethium-151 Pm [151Pm] 150.92122
10130012 promethium-142 Pm [142Pm] 141.9129
16048796 promethium-153 Pm [153Pm] 152.92416

Isotopes

Stable Isotope Count 0

Isotopes in Industry

The beta-particle-emitting isotope 147Pm (with a half-life of 2.68 years) is used in the nuclear fuel industry to measure the thickness of the inner surface layer of graphite in the cladding tube where the nuclear fuel rod is placed in a nuclear fuel reactor (Fig. IUPAC.61.1). The graphite serves as a protective layer against mechanical contact between the nuclear fuel rod and the Zircaloy cladding (fuel-rod holding tube) and as a diffusion barrier against fission products. By placing a layer of 147Pm along the inner surface of the cladding before the graphite, the long half-life of 147Pm and constant beta-particle emission provide a reliable and simple technique to measure the thickness of the graphite along the inner surface of the tube (called the beta-ray backscatter technique) [432], [433], [434].

The beta decay property of 147Pm makes this radioisotope an ideal candidate for nuclear batteries (beta voltaics). Long-lived power supplies for remote and sometimes hostile environmental conditions are needed for space and sea missions, and nuclear batteries can uniquely serve this role. A nuclear battery using beta voltaics can have an energy density (quantity of energy per unit mass) near a thousand watt-h per kilogram with 21 percent efficiency, which is much greater than the best chemical batteries [435].

Fig. IUPAC.61.1: The beta-ray backscatter technique requires a layer of ¹⁴⁷Pm between the cladding and the graphite layer to measure the thickness of the graphite along the inner surface of the cladding tube. (Modified from [308]).

[308] Whatisnuclear.com. Nuclear Reactors, Whatisnuclear.com (2014), Feb. 26; http://www.whatisnuclear.com/articles/nucreactor.html.
[432] J. K. Shultis, R. E. Faw. Fundamentals of Nuclear Science and Engineering, Marcel Dekker, Inc., New York (2002).
[433] M. Kumar, J. Udhayakumar, J. Nuwad, R. Shukla, C. G. S. Pillai, A. Dash, M. Venkatesh. Appl. Radiat. Isot.69, 580 (2011).
[434] R. P. Taleyarkhan. Atoms for Peace: an International Journal.2, 381 (2009).
[435] G. N. Yakubova. “Nuclear batteries with tritium and promethium-147 radioactive sources”, Ph.D dissertation, Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Illinois, USA (2010). http://hdl.handle.net/2142/16849.

Isotope Mass and Abundance

Isotope Atomic Mass (uncertainty) [u] Abundance (uncertainty)
145Pm 144.9127559(33)
147Pm 146.9151450(19)

Atomic Mass, Half Life, and Decay

Nuclide Atomic Mass and Uncertainty [u] Half Life and Uncertainty Discovery Year Decay Modes, Intensities and Uncertainties [%]
126Pm 125.957327 ± 0.000537 [Estimated] 500 ms [Estimated] β+ ?; β+p ?
127Pm 126.951358 ± 0.000429 [Estimated] 1 s [Estimated] β+ ?; p ?
128Pm 127.948234 ± 0.000322 [Estimated] 1.0 s ± 0.3 1999 β+≈100%; β+p= ?; p=0%
129Pm 128.942909 ± 0.000322 [Estimated] 2.4 s ± 0.9 2004 β+=100%; β+p ?; p ?
130Pm 129.940451 ± 0.000215 [Estimated] 2.6 s ± 0.2 1985 β+=100%; β+p=?
131Pm 130.935834 ± 0.000215 [Estimated] 6.3 s ± 0.8 1998 β+=100%
132Pm 131.933840 ± 0.00016 [Estimated] 6.2 s ± 0.6 1977 β+=100%; β+p≈5e-5%
133Pm 132.929782000 ± 0.000054 13.5 s ± 2.1 1977 β+=100%
133Pmm 132.929782000 ± 0.000054 8 s [Estimated] 1996 β+ ?; IT ?
134Pm 133.928326000 ± 0.000045 22 s ± 1 1977 β+=100%
134Pmm 133.928326000 ± 0.000045 ~5 s 1988 β+=100%
134Pmn 133.928326000 ± 0.000045 20 us ± 1 2009 IT=100%
135Pm 134.924785000 ± 0.000089 49 s ± 3 1975 β+=100%
135Pmm 134.924785000 ± 0.000089 40 s ± 3 1989 β+=100%
136Pm 135.923595949 ± 0.000074152 107 s ± 6 1988 β+=100%
136Pmm 135.923595949 ± 0.000074152 90 s ± 35 1982 β+=100%
136Pmn 135.923595949 ± 0.000074152 1.5 us ± 0.1 1987 IT=100%
137Pm 136.920479519 ± 0.000014 2 m [Estimated] 1975 β+ ?
137Pmm 136.920479519 ± 0.000014 2.4 m ± 0.1 1973 β+=100%
138Pm 137.919576119 ± 0.000012456 3.24 m ± 0.05 1973 β+=100%
138Pmm 137.919576119 ± 0.000012456 10 s ± 2 β+=100%
139Pm 138.916799228 ± 0.000014587 4.15 m ± 0.05 1967 β+=100%
139Pmm 138.916799228 ± 0.000014587 180 ms ± 20 1975 IT≈100%; β+ ?
140Pm 139.916035918 ± 0.000026001 9.2 s ± 0.2 1966 β+=100%
140Pmm 139.916035918 ± 0.000026001 5.95 m ± 0.05 1966 β+=100%
141Pm 140.913555081 ± 0.000015 20.90 m ± 0.05 1952 β+=100%
141Pmm 140.913555081 ± 0.000015 630 ns ± 20 1970 IT=100%
141Pmn 140.913555081 ± 0.000015 >2 us 1985 IT=100%
142Pm 141.912890982 ± 0.00002533 40.5 s ± 0.5 1959 β+=100%; e+=77.1±2.7%; ε=22.9±2.7%
142Pmm 141.912890982 ± 0.00002533 2.0 ms ± 0.2 1971 IT=100%
142Pmn 141.912890982 ± 0.00002533 67 us ± 5 1974 IT=100%
143Pm 142.910938068 ± 0.00000316 265 d ± 7 1952 ε=100%; e+<5.7e-6%
144Pm 143.912596208 ± 0.000003126 363 d ± 14 1952 ε=100%; e+<8e-5%
144Pmm 143.912596208 ± 0.000003126 780 ns ± 200 1993 IT=100%
144Pmn 143.912596208 ± 0.000003126 ~2.7 us 1994 IT=100%
145Pm 144.912755748 ± 0.000003011 17.7 y ± 0.4 1951 ε=100%; α=2.8e-7%
146Pm 145.914702240 ± 0.000004589 5.53 y ± 0.05 1960 ε=66.0±1.3%; β-=34.0±1.3%
147Pm 146.915144944 ± 0.000001382 2.6234 y ± 0.0002 1947 β-=100%
148Pm 147.917481091 ± 0.000006108 5.368 d ± 0.007 1947 β-=100%
148Pmm 147.917481091 ± 0.000006108 41.29 d ± 0.11 1951 β-=95.8±0.6%; IT=4.2±0.6%
149Pm 148.918341507 ± 0.000002344 53.08 h ± 0.05 1947 β-=100%
149Pmm 148.918341507 ± 0.000002344 35 us ± 3 1966 IT=100%
150Pm 149.920990014 ± 0.000021504 2.698 h ± 0.015 1952 β-=100%
151Pm 150.921216613 ± 0.000004949 28.40 h ± 0.04 1952 β-=100%
152Pm 151.923505185 ± 0.000027809 4.12 m ± 0.08 1958 β-=100%
152Pmm 151.923505185 ± 0.000027809 7.52 m ± 0.08 1971 β-=100%
152Pmn 151.923505185 ± 0.000027809 13.8 m ± 0.2 1971 β-=100%; IT ?
153Pm 152.924156252 ± 0.000009729 5.25 m ± 0.02 1962 β-=100%
154Pm 153.926712791 ± 0.000026861 2.68 m ± 0.07 1958 β-=100%
154Pmm 153.926712791 ± 0.000026861 1.73 m ± 0.10 1958 β-=100%
155Pm 154.928136951 ± 0.000005065 41.5 s ± 0.2 1982 β-=100%
156Pm 155.931114059 ± 0.000001275 27.4 s ± 0.5 1986 β-=100%
156Pmm 155.931114059 ± 0.000001275 2.3 s ± 2.0 2007 IT≈98%; β-≈2%
157Pm 156.933121298 ± 0.000007521 10.56 s ± 0.10 1987 β-=100%
158Pm 157.936546948 ± 0.000000953 4.8 s ± 0.5 1987 β-=100%
158Pmm 157.936546948 ± 0.000000953 >16 us 2015 IT=?; β- ?
159Pm 158.939286409 ± 0.000010777 1.49 s ± 0.13 1998 β-=100%
159Pmm 158.939286409 ± 0.000010777 4.42 us ± 0.17 2015 IT=100%
160Pm 159.943215272 ± 0.0000022 725 ms ± 57 2012 β-=100%; β-n ?
160Pmm 159.943215272 ± 0.0000022 >700 ms 2020 β- ?; IT ?; β-n ?
161Pm 160.946229837 ± 0.0000097 1.05 s ± 0.15 2012 β-=100%; β-n ?
161Pmm 160.946229837 ± 0.0000097 0.89 us ± 0.09 2015 IT=100%
162Pm 161.950574 ± 0.000322 [Estimated] 630 ms ± 180 2012 β-=100%; β-n ?
163Pm 162.953881 ± 0.000429 [Estimated] 255 ms ± 25 2012 β-=100%; β-n ?
164Pm 163.958819 ± 0.000429 [Estimated] 300 ms >550ns [Estimated] 2018 β- ?; β-n ?
165Pm 164.962780 ± 0.000537 [Estimated] 260 ms >550ns [Estimated] 2018 β- ?; β-n ?

Information Sources

  1. 1.  PubChem
  2. 2.  Atomic Mass Data Center (AMDC), International Atomic Energy Agency (IAEA)
  3. 3.  IUPAC Commission on Isotopic Abundances and Atomic Weights (CIAAW)
  4. 4.  IUPAC Periodic Table of the Elements and Isotopes (IPTEI)
    LICENSE
    Copyright (c) 2020 International Union of Pure and Applied Chemistry. The International Union of Pure and Applied Chemistry (IUPAC) contribution within Pubchem is provided under a CC-BY-NC-ND 4.0 license, unless otherwise stated.
    https://creativecommons.org/licenses/by-nc-nd/4.0/
  5. 5.  Jefferson Lab, U.S. Department of Energy
    LICENSE
    Please see citation and linking information https https://www.jlab.org/privacy-and-security-notice
  6. 6.  Los Alamos National Laboratory, U.S. Department of Energy
  7. 7.  NIST Physical Measurement Laboratory
  8. 8.  PubChem Elements
    Promethium

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