Curium

This article is about the chemical element Curium; for the ancient city also called Curium (located in Cyprus), see Kourion
96 americiumcuriumberkelium
Gd

Cm

(Uqh)
Cm-TableImage.png
Periodic Table - Extended Periodic Table
General
Name, Symbol, Number curium, Cm, 96
Element category actinides
Group, Period, Block n/a, 7, f
Appearance silvery
Standard atomic weight (247)  g·mol−1
Electron configuration [Rn] 5f7 6d1 7s2
Electrons per shell 2, 8, 18, 32, 25, 9, 2
Physical properties
Phase solid
Density (near r.t.) 13.51  g·cm−3
Melting point 1613 K
(1340 °C, 2444 °F)
Boiling point 3383 K
(3110 °C, 5630 °F)
Heat of fusion  ? 15  kJ·mol−1
Vapor pressure
P(Pa) 1 10 100 1 k 10 k 100 k
at T(K) 1788 1982        
Atomic properties
Crystal structure hexagonal close-packed
Oxidation states 3
(amphoteric oxide)
Electronegativity 1.3 (Pauling scale)
Ionization energies 1st: 581 kJ/mol
Miscellaneous
Magnetic ordering no data
CAS registry number 7440-51-9
Most-stable isotopes
Main article: Isotopes of curium
iso NA half-life DM DE (MeV) DP
242Cm syn 160 days SF - -
α 6.1 238Pu
243Cm syn 29.1 y α 6.169 239Pu
ε 0.009 243Am
SF - -
244Cm syn 18.1 y SF - -
α 5.902 240Pu
245Cm syn 8500 y SF - -
α 5.623 241Pu
246Cm syn 4730 y α 5.475 242Pu
SF - -
247Cm syn 1.56×107 y α 5.353 243Pu
248Cm syn 3.40×105 y α 5.162 244Pu
SF - -
250Cm syn 9000 y SF - -
α 5.169 246Pu
β- 0.037 250Bk
References

Curium (pronounced /ˈkjuːriəm/) is a synthetic chemical element with the symbol Cm and atomic number 96. A radioactive metallic transuranic element of the actinide series, curium is produced by bombarding plutonium with alpha particles (helium ions) and was named for Marie Curie and her husband Pierre.

Contents

Characteristics

The isotope curium-248 has been synthesized only in milligram quantities, but curium-242 and curium-244 are made in multigram amounts, which allows for the determination of some of the element's properties. Curium-244 can be made in quantity by subjecting plutonium to neutron bombardment. Curium does not occur in nature. There are few commercial applications for curium but it may one day be useful in radioisotope thermoelectric generators. Curium bio-accumulates in bone tissue where its radiation destroys bone marrow and thus stops red blood cell creation.

A rare earth homolog, curium is somewhat chemically similar to gadolinium but with a more complex crystal structure. Chemically reactive, its metal is silvery-white in color and the element is more electropositive than aluminium (most trivalent curium compounds are slightly yellow).

Curium has been studied greatly as a potential fuel for radioisotope thermoelectric generators (RTG). Curium-242 can generate up to 120 watts of thermal energy per gram (W/g); however, its very short half-life makes it undesirable as a power source for long-term use. Curium-242 can decay by alpha emission to plutonium-238 which is the most common fuel for RTGs. Curium-244 has also been studied as an energy source for RTGs having a maximum energy density ~3 W/g[1], but produces a large amount of neutron radiation from spontaneous fission. Curium-243 with a ~30 year half-life and good energy density of ~1.6 W/g would seem to make an ideal fuel, but it produces significant amounts of gamma and beta radiation from radioactive decay products.

Compounds

Some compounds are:

History

Glenn T. Seaborg

Curium was first synthesized at the University of California, Berkeley by Glenn T. Seaborg, Ralph A. James, and Albert Ghiorso in 1944.[2] The team named the new element after Marie Curie and her husband Pierre who are famous for discovering radium and for their work in radioactivity. It was chemically identified at the Metallurgical Laboratory (now Argonne National Laboratory) at the University of Chicago. It was actually the third transuranium element to be discovered even though it is the fourth in the series. Curium-242 (half-life 163 days) and one free neutron were made by bombarding alpha particles onto a plutonium-239 target in the 60-inch cyclotron at Berkeley.[3] Louis Werner and Isadore Perlman created a visible sample of curium-242 hydroxide at the University of California in 1947 by bombarding americium-241 with neutrons.[4] Curium was made in its elemental form in 1951 for the first time.[5][6]

Isotopes

19 radioisotopes of curium have been characterized, with the most stable being Cm-247 with a half-life of 1.56 × 107 years, Cm-248 with a half-life of 3.40 × 105 years, Cm-250 with a half-life of 9000 years, and Cm-245 with a half-life of 8500 years. All of the remaining radioactive isotopes have half-lives that are less than 30 years, and the majority of these have half-lives that are less than 33 days. This element also has 4 meta states, with the most stable being Cm-244m (t½ 34 ms). The isotopes of curium range in atomic weight from 233.051 u (Cm-233) to 252.085 u (Cm-252).

Nuclear fuel cycle

Transmutation flow between 238Pu and 244Cm in LWR.[7]
Fission percentage is 100 minus shown percentages.
Total rate of transmutation varies greatly by nuclide.
245Cm–248Cm are long-lived with negligible decay.
Thermal neutron cross sections
242Cm 243Cm 244Cm 245Cm 246Cm 247Cm
Fission 5 617 1.04 2145 0.14 81.90
Capture 16 130 15.20 369 1.22 57
C/F ratio 3.20 0.21 14.62 0.17 8.71 0.70
LEU spent fuel 20 years after 53 MWd/kg burnup[8]
3 common isotopes 51 3700 390
Fast reactor MOX fuel (avg 5 samples, burnup 66-120GWd/t)[9]
Total curium 3.09×10-3% 27.64% 70.16% 2.166% 0.0376% 0.000928%

The odd-mass number isotopes are fissile, the even-mass number isotopes are not and can only neutron capture, but very slowly. Therefore in a thermal reactor the even-mass isotopes accumulate as burnup increases.

The MOX which is to be used in power reactors should contain little or no curium as the neutron activation of 248Cm will create californium which is a strong neutron emitter. The californium would pollute the back end of the fuel cycle and increase the dose to workers. Hence if the minor actinides are to be used as fuel in a thermal neutron reactor, the curium should be excluded from the fuel or placed in special fuel rods where it is the only actinide present.

References

  1. Gmelins Handbuch der anorganischen Chemie, System Nr. 71, Band 7 a, Transurane, Teil A 2, p. 289.
  2. Hall, Nina (2000). The New Chemistry: A Showcase for Modern Chemistry and Its Applications. Cambridge University Press. pp. 8–9. ISBN 9780521452243. http://books.google.com/books?id=U4rnzH9QbT4C. 
  3. G. T. Seaborg, R. A. James, A. Ghiorso: "The New Element Curium (Atomic Number 96)", NNES PPR (National Nuclear Energy Series, Plutonium Project Record), Vol. 14 B, The Transuranium Elements: Research Papers, Paper No. 22.2, McGraw-Hill Book Co., Inc., New York, 1949; Abstract; Typoskript (January 1948).
  4. L. B. Werner, I. Perlman: "Isolation of Curium", NNES PPR (National Nuclear Energy Series, Plutonium Project Record), Vol. 14 B, The Transuranium Elements: Research Papers, Paper No. 22.5, McGraw-Hill Book Co., Inc., New York, 1949.
  5. J. C. Wallmann, W. W. T. Crane, B. B. Cunningham: "The Preparation and Some Properties of Curium Metal", in: J. Am. Chem. Soc. 1951, 73 (1), 493–494; doi:10.1021/ja01145a537.
  6. L. B. Werner, I. Perlman: "First Isolation of Curium", in: J. Am. Chem. Soc. 1951, 73 (11), 5215–5217; doi:10.1021/ja01155a063.
  7. Sasahara, Akihiro (April 2004). "Neutron and Gamma Ray Source Evaluation of LWR High Burn-up UO2 and MOX Spent Fuels". Journal of NUCLEAR SCIENCE and TECHNOLOGY 41 (4): 448–456. doi:10.3327/jnst.41.448. http://www.jstage.jst.go.jp/article/jnst/41/4/448/_pdf. 
  8. "Limited Proliferation-Resistance Benefits from Recycling Unseparated Transuranics and Lanthanides from Light-Water Reactor Spent Fuel" (PDF).
  9. "Analysis of Curium Isotopes in Mixed Oxide Fuel Irradiated in Fast Reactor" (PDF).

Literature

External links