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Plutonium–gallium alloy (9174 views - Material Database)

Plutonium–gallium alloy (Pu–Ga) is an alloy of plutonium and gallium, used in nuclear weapon pits, the component of a nuclear weapon where the fission chain reaction is started. This alloy was developed during the Manhattan Project.
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Plutonium–gallium alloy

Plutonium–gallium alloy

Plutonium–gallium alloy (Pu–Ga) is an alloy of plutonium and gallium, used in nuclear weapon pits, the component of a nuclear weapon where the fission chain reaction is started. This alloy was developed during the Manhattan Project.


Metallic plutonium has several different solid allotropes. The δ phase is the least dense and most easily machinable. It is formed at temperatures of 310–452 °C at ambient pressure (1 atmosphere), and is thermodynamically unstable at lower temperatures. However, plutonium can be stabilized in the δ phase by alloying it with a small amount of another metal. The preferred alloy is 3.0–3.5 mol.% (0.8–1.0 wt.%) gallium.

Pu–Ga has many practical advantages:[1]

  • stable between −75 to 475 °C,
  • very low thermal expansion,
  • low susceptibility to corrosion (4% of the corrosion rate of pure plutonium),
  • good castability; since plutonium has the rare property that the molten state is denser than the solid state, the tendency to form bubbles and internal defects is decreased.

Use in nuclear weapons

Stabilized δ-phase Pu–Ga is ductile, and can be rolled into sheets and machined by conventional methods. It is suitable for shaping by hot pressing at about 400 °C. This method was used for forming the first nuclear weapon pits.

More modern pits are produced by casting. Subcritical testing showed that wrought and cast plutonium performance is the same.[2][3] As only the ε-δ transition occurs during cooling, casting Pu-Ga is much less problematic than casting pure plutonium.[4]

δ phase Pu–Ga is still thermodynamically unstable, so there are concerns about its aging behavior. There are substantial differences of density (and therefore volume) between the various phases. The transition between δ-phase and α-phase plutonium occurs at a low temperature of 115 °C and can be reached by accident. Prevention of the phase transition and the associated mechanical deformations and consequent structural damage and/or loss of symmetry is of critical importance. Under 4 mol.% gallium the pressure-induced phase change is irreversible.

However, the phase change is useful during the operation of a nuclear weapon. As the reaction starts, it generates enormous pressures, in the range of hundreds of gigapascals. Under these conditions, δ phase Pu–Ga transforms to α phase, which is 25% denser and thus more critical.

Effect of gallium

Plutonium in its α phase has a low internal symmetry, caused by uneven bonding between the atoms, more resembling (and behaving like) a ceramic than a metal. Addition of gallium causes the bonds to become more even, increasing the stability of the δ phase.[5] The α phase bonds are mediated by the 5f shell electrons, and can be disrupted by increased temperature or by presence of suitable atoms in the lattice which reduce the available number of 5f electrons and weaken their bonds.[6] The alloy is more dense in molten state than in solid state, which poses an advantage for casting as the tendency to form bubbles and internal defects is decreased.[1][7]

Gallium tends to segregate in plutonium, causing "coring"—gallium-rich centers of grains and gallium-poor grain boundaries. To stabilize the lattice and reverse and prevent segregation of gallium, annealing is required at the temperature just below the δ–ε phase transition, so gallium atoms can diffuse through the grains and create homogeneous structure. The time to achieve homogenization of gallium increases with increasing grain size of the alloy and decreases with increasing temperature. The structure of stabilized plutonium at room temperature is the same as unstabilized at δ-phase temperature, with the difference of gallium atoms substituting plutonium in the fcc lattice.

The presence of gallium in plutonium signifies its origin from weapon plants or decommissioned nuclear weapons. The isotopic signature of plutonium then allows rough identification of its origin, manufacturing method, type of the reactor used in its production, and rough history of the irradiation, and matching to other samples, which is of importance in investigation of nuclear smuggling.[8]


There are several plutonium and gallium intermetallic compounds: PuGa, Pu3Ga, and Pu6Ga.

During aging of the stabilized δ alloy, gallium segregates from the lattice, forming regions of Pu3Ga (ζ'-phase) within α phase, with the corresponding dimensional and density change and buildup of internal strains. The decay of plutonium however produces energetic particles (alpha particles and uranium-235 nuclei) that cause local disruption of the ζ' phase, and establishing a dynamic equilibrium with only a modest amount of ζ' phase present, which explains the alloy's unexpectedly slow, graceful aging.[9][10] The alpha particles are trapped as interstitial helium atoms in the lattice, coalescing into tiny (about 1 nm diameter) helium-filled bubbles in the metal and causing negligible levels of void swelling; the size of bubbles appears to be limited, though their number increases with time.

Addition of 7.5 wt.% of plutonium-238, which has significantly faster decay rate, to the alloy increases the aging damage rate by 16 times, assisting with plutonium aging research. The Blue Gene supercomputer aided with simulations of plutonium aging processes.[11]


Plutonium alloys can be produced by adding a metal to molten plutonium. However, if the alloying metal is sufficiently reductive, plutonium can be added in the form of oxides or halides. The δ phase plutonium–gallium and plutonium–aluminium alloys are produced by adding plutonium(III) fluoride to molten gallium or aluminium, which has the advantage of avoiding dealing directly with the highly reactive plutonium metal.[12]

Reprocessing into MOX fuel

For reprocessing of surplus warhead pits into MOX fuel, the majority of gallium has to be removed as its high content could interfere with the fuel rod cladding (gallium attacks zirconium[13]) and with migration of fission products in the fuel pellets. In the ARIES process, the pits are converted to oxide by converting the material to plutonium hydride, then optionally to nitride, and then to oxide. Gallium is then mostly removed from the solid oxide mixture by heating at 1100 °C in a 94% argon 6% hydrogen atmosphere, reducing gallium content from 1% to 0.02%. Further dilution of plutonium oxide during the MOX fuel manufacture brings gallium content to levels considered negligible. A wet route of gallium removal, using ion exchange, is also possible.[14] Electrorefining is another way to separate gallium and plutonium.[15]

Development history

During the Manhattan Project, the maximum amount of diluent atoms for plutonium to not affect the explosion efficiency was calculated to be 5 mol.%. Two stabilizing elements were considered, silicon and aluminium. However, only aluminium produced satisfactory alloys. But the aluminium tendency to react with α-particles and emit neutrons limited its maximum content to 0.5 mol.%; the next element from the boron group of elements, gallium, was tried and found satisfactory.[16][17]

  1. ^ a b "The drama of plutonium". Nuclear Engineering International. 2005. Retrieved 2010-01-25. 
  2. ^ "Italian Stallions & Plutonium". jeffrey. Retrieved 2010-01-25. 
  3. ^ "Optical Pyrometry on the Armando Subcritical Experiment". Los Alamos National Laboratory. Retrieved 2010-01-25. 
  4. ^ "Plutonium (Pu)". centurychina.com. Archived from the original on January 7, 2010. Retrieved 2010-01-25. 
  5. ^ "Scientists tackle long-standing questions about plutonium". innovations-report. 2006. Retrieved 2010-01-25. 
  6. ^ Hecker, Siegfried S. (2000). "Plutonium and Its Alloys" (PDF). Los Alamos Science Number 26. Retrieved 2010-01-25. 
  7. ^ Darby, Richard. "Modelling the Lattice Parameter of Plutonium Aluminium Solid Solution" (PDF). Retrieved 2010-01-25. 
  8. ^ Edwards, Rob (19 August 1995). "Fissile Fingerprints". New Scientist. Retrieved 2010-01-25. 
  9. ^ Martz, Joseph C.; Schwartz, Adam J. "Plutonium: Aging Mechanisms and Weapon Pit Lifetime Assessment". The Minerals, Metals & Materials Society. Retrieved 2010-01-25. 
  10. ^ Wolfer, W. G.; Oudot, B.; Baclet, N. (2006). "Reversible expansion of gallium-stabilized δ-plutonium". Journal of Nuclear Materials. 359 (3): 185–191. Bibcode:2006JNuM..359..185W. doi:10.1016/j.jnucmat.2006.08.020. 
  11. ^ "U.S. Weapons Plutonium Ages Gracefully". Science and Technology Reviews. Retrieved 2010-01-25. 
  12. ^ Moody, Kenton James; Hutcheon, Ian D.; Grant, Patrick M. (2005-02-28). Nuclear forensic analysis. CRC Press. ISBN 978-0-8493-1513-8. 
  13. ^ "Gallium Interactions with Zircaloy Cladding" (PDF). Amarillo National Resource Center for Plutonium. Retrieved 2010-01-25. 
  14. ^ Toevs, James W.; Beard, Carl A. "Gallium in Weapons-Grade Plutonium and MOX Fuel Fabrication". IEEE. Retrieved 2010-01-25. 
  15. ^ "Method for plutonium-gallium separation by anodic dissolution of a solid plutonium-gallium alloy". frepatent. Retrieved 2010-01-25. 
  16. ^ "First Nuclear Weapons: Nuclear Weapons Frequently Asked Questions". nuclearweaponarchive.org. Retrieved 2010-01-25. 
  17. ^ "Dr Smith goes to Los Alamos" (PDF). RESONANCE. June 2006. Retrieved 2010-01-25. 

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