A microscopic sample of plutonium was first isolated by Glenn Seaborg in August 1942 as part of the
Manhattan Project. The first-milligram quantities were not created in a reactor, but by the
irradiation of uranyl nitrate solution by the cyclotron at the University of California at
Berkeley, US.
In December 1944 the construction of the chemical
separation plants at Hanford were finished, and on February 2, 1945, Los Alamos received its first
plutonium.
Plutonium is a highly carcinogenic, radioactive substance
which does not exist in the natural environment and is only produced artificially in nuclear
reactors. It is made by the irradiation with neutrons of uranium-238 in military as well as
civilian nuclear reactors. Plutonium has 15 isotopes with mass numbers ranging from 232 to 246.
Only two plutonium isotopes have military and commercial applications:
The plutonium isotopes 240, 241 and 242 have no commercial application and are merely
contaminants.
The formed plutonium is contained inside the spent fuel rods. The longer the fuel is inside the
reactor, the more contaminant plutonium isotopes are formed. In military reactors the fuel is
replaced after some weeks in order to obtain as much plutonium-239 as possible. In commercial
reactors this is done after three to four years.
The minimal amount of nuclear material necessary to sustain a chain reaction is called the critical
mass. The smallest theoretical critical mass of Pu-239 is a few hundred grams.
The amount of plutonium used in fission weapons is in the 3-5 kg range.
Plutonium has been classified into grades by the US Department of Energy (DOE)
This classification is, however, somewhat misleading. Fuel grade and reactor grade may be less
suitable but still can be made into a nuclear weapon. There have been at least two known nuclear
weapon tests with civil plutonium. In 1953, Britain exploded a 12-kiloton bomb, named Totem I, at
one of their test sites in Australia.6 In 1962, the US conducted an
underground test with reactor grade plutonium at the Nevada test site.7
During reprocessing, plutonium is separated from spent nuclear fuel. Reprocessing has pure military
origins. Development of this technology dates back to the US of 1944, to the Manhattan Project
whose only goal was the developing and production of the nuclear bomb. The plutonium was produced
in dedicated military reactors with low-burn-up fuel. Fuel in power reactors is irradiated for
longer periods to reach a higher burn-up, because the fuel irradiation generates the heat for the
electricity production. The military purpose is the production of plutonium and therefore the
burn-up is kept low to produce a plutonium-239 as pure as possible. It is important to keep the
presence of higher isotopes, particularly plutonium-240, to a minimum.
8
Reprocessing plants handle spent fuel mechanically and chemically in order to separate plutonium
from mainly uranium and other fission products. Reprocessing is an extremely polluting technique
mainly due to massive radioactive releases in air and water.
Civil reprocessing was applied on an experimental scale from 1966-1974 by the Eurochemic
reprocessing plant in Dessel, Belgium, and from 1972-1990 by the WAK in Karlsruhe, Germany. From
the late 1960s on, large scale reprocessing of spent fuel from commercial nuclear power plants
started: in France the Marcoule plant UP1 (1958-1997) and La Hague UP2 (1966-1976); in the UK
Windscale B-204 from 1969-1973; and in the US, West Valley (1966-1972).
9 The two largest reprocessors and plutonium companies in the world are British
Nuclear Fuel Ltd. (BNFL) and the French Compagnie Générale des Matières
Nucléaires (Cogéma). Based on the nominal production capacity of 1600 MT/year for La
Hague
10 and 900 MT/y for Sellafield
11
the maximum Pu production in the next 20 years will be about 500,000 kg Pu on the assumption of an
average of 1% Pu in the spent fuel.
Table 2.3 Estimated civil world plutonium production12
| Country |
Plant |
Prod. Cap. spent fuel (ton/yr) |
Max. Pu. prod. (kg/yr) |
Start-up |
| India |
Tarapur |
100 |
1.000 |
1982 |
| Kalpakkam |
100 |
1.000 |
1996 |
| Japan |
Tokai-Mura |
90 |
900 |
1977 |
| France |
UP-2 800 |
850 |
8.500 |
1994 |
| UP-3 |
800 |
8.000 |
1990 |
| Russia |
RT-1, Mayak13 |
400 |
2.500 |
1977 |
| UK |
THORP |
700 |
7.000 |
1997 |
| B-205 MAGNOX |
1.500 |
4.500 |
1964 |
| Maximum total annual Pu production |
33.400 |
At present, about half of the annual plutonium production in civil nuclear fuel is separated in
reprocessing plants. Each year about 60,000 kg of plutonium is produced in nuclear reactors, from
which about half (some 33,400 kg) of plutonium is separated.
The estimated cumulative civil plutonium production in civil nuclear reactors until the end of
1995 is about a million kg of plutonium, from which about 800,000 kg is inside the spent fuel.
About 190,000 kg of plutonium has been reprocessed. Of this plutonium 141,000 kg is stockpiled and
49,000 kg is recycled as MOX fuel in LWRs and FBRs.14
The amount of civil separated plutonium will increase enormously. The next 20 years the
cumulative production of civil reprocessing plants will be about 600,000 kg of plutonium. This is
twice the total military plutonium production from World War II till now.
The five official nuclear weapon countries -- the US, Russia, Great Britain, China and France --
have produced an estimated 300,000-kg plutonium in the past 50 years. In the US all 14 military
reactors were closed by 1988. By then the reactors had produced about 100,000 kg weapon-grade
plutonium and 11,000-kg fuel- and reactor-grade plutonium.
15 In the
USSR an estimated 177,000 kg of military plutonium were produced by 13 military reactors and
separated by the end of 1993. Only three military reactors are still in operation.
16 Since about 1985, some 10 thousands of nuclear weapons have been
dismantled. As a result, the stocks of weapon-grade plutonium are increasing. Both the US and
Russia declared about 50,000-kg plutonium each as surplus stocks. The UK, France and China together
produced and separated about 12,000-kg weapon-grade plutonium.
17
Sources:
- IPPNW/IEER, 'Plutonium Deadly gold of the Nuclear Age',
Cambridge, 1992, p.3
- US Department of Energy, 'The Manhattan Project; Making The Atomic
Bomb', Oak Ridge, September 1994, p.64
- IEER fact sheet, 'Physical, Nuclear and Chemical Properties of
Plutonium', Washington, October 1994, p.1
- IEER fact sheet, 'Physical, Nuclear and Chemical Properties of
Plutonium', Washington, October 1994, p.2
- Cochran, T.B., W.M.Arkin, R.S.Norris, M.M.Hoenig; 'Nuclear Weapons
Databook, Vol. II U.S. Nuclear Warhead Facility Profiles', Cambridge, Ballinger Publishing
Company, 1987, p.136
- Hawkes, N., a.o, 'The Worst Accident in the World', London
Observer, 1986, p.58,59
- DOE Facts, 'Additional Information Concerning Underground Nuclear
Weapon Test of Reactor-grade Plutonium', Washington, June 1994
- IEER fact sheet, 'Physical, Nuclear and Chemical Properties of
Plutonium', Washington, October 1994, p.3
- Albright, D., F.Berkhout, W.Walker, 'World Inventory of Plutonium
and Highly Enriched Uranium 1992', Oxford University Press, 1993, p.90
- Nuclear Fuel, 1 January 1996; La Hague site reaches nominal
production; MELOX gears up, p.12
- Nuclear Fuel, 17 June 1996: 'Hundreds of Japanese flock to THORP
as plant gears up for full operation', p.19-20
- Energy & Security, No.2 1997; 'Reprocessing: Where and
How', p.8-9
- Nuclear Fuel, 1 January 1996, 'RT-1 operation faces cost crisis,
uncertain future demand schedule', p.10
- Energy and Security, No.2 1997; 'World Civilian plutonium
inventories', p.14
- Albright, D., F.Berkhout, W.Walker; 'World Inventory of Plutonium
and Highly Enriched Uranium 1992', Oxford University Press, 1993, p.34
- Böhmer, N., T.Nilsen; 'Reprocessing Plants in Siberia',
Bellona Working Paper, 19 September 1995, Oslo, p.2
- Albright, D., F.Berkhout, W.Walker; 'World Inventory of Plutonium
and Highly Enriched Uranium 1992', Oxford University Press, 1993, p.41-46