Uranium-233 ( or U-233) is a fissile isotope of uranium that is bred from thorium-232 as part of the thorium fuel cycle. Uranium-233 was investigated for use in nuclear weapons and as a reactor fuel.
Fissile material
thumb|right|[[Molten-Salt Reactor Experiment]]
thumb|right|[[Shippingport Atomic Power Station]]
thumb|right|German [[THTR-300]]
In 1946, the public first became informed of uranium-233 bred from thorium as "a third available source of nuclear energy and atom bombs" (in addition to uranium-235 and plutonium-239), following a United Nations report and a speech by Glenn T. Seaborg.
The United States produced, over the course of the Cold War, approximately 2 metric tons of uranium-233, in varying levels of chemical and isotopic purity. These were produced at the Hanford Site and Savannah River Site in reactors that were designed for the production of plutonium-239.
Nuclear fuel
Uranium-233 has been used as a fuel in several different reactor types, and is proposed as a fuel for several new designs (see thorium fuel cycle), all of which breed it from thorium. Uranium-233 can be bred in either fast reactors or thermal reactors, unlike the uranium-238-based fuel cycles which require the superior neutron economy of a fast reactor in order to breed plutonium, that is, to produce more fissile material than is consumed.
The long-term strategy of the nuclear power program of India, which has substantial thorium reserves, is to move to a nuclear program breeding uranium-233 from thorium feedstock.
Energy released
The fission of one atom of uranium-233 generates 197.9 MeV = 3.171·10<sup>−11</sup> J (i.e. 19.09 TJ/mol = 81.95 TJ/kg = 22764 MWh/kg that is 1.8 million times more than the same mass of diesel).
{| class="wikitable" style="text-align:center"
! Source !! Average energy<br />released (MeV)
|-
|colspan="2" style="background:#88F; color:#FFF;"|Instantaneously released energy
|-
|Kinetic energy of fission fragments||style="background:#DFD;" style="text-align:center"| 168.2
|-
|Kinetic energy of prompt neutrons||style="background:#DFD;" style="text-align:center"| 4.8
|-
|Energy carried by prompt γ-rays||style="background:#DFD;" style="text-align:center"| 7.7
|-
|colspan="2" style="background:#88F; color:#FFF;"|Energy from decaying fission products
|-
|Energy of β<sup>−</sup> particles||style="background:#DFD;" style="text-align:center"| 5.2
|-
|Energy of anti-neutrinos|| style="color:#AAA;" style="text-align:center"| 6.9
|-
|Energy of delayed γ-rays ||style="background:#DFD;" style="text-align:center"| 5.0
|-
|style="background:#F44;color:#FFF;"|Sum (excluding escaping anti-neutrinos)||style="background:#F44;color:#FFF;" style="text-align:center"| 191.0
|-
|Energy released when those prompt neutrons which don't (re)produce fission are captured||style="background:#DFD;" style="text-align:center"| 9.1
|-
|style="background:#777;color:#FFF;"|Energy converted into heat in an operating thermal nuclear reactor||style="background:#777;color:#FFF;" style="text-align:center"| 200.1
|}
Weapon material
thumb|right|The first detonation of a nuclear bomb that included U-233, on 15 April 1955
As a potential weapon material, pure uranium-233 is more similar to plutonium-239 than uranium-235 in terms of source (bred vs natural), half-life and critical mass (both 4–5 kg in beryllium-reflected sphere). Unlike reactor-bred plutonium, it has a very low spontaneous fission rate, which combined with its low critical mass made it initially attractive for compact gun-type weapons, such as small-diameter artillery shells.
A declassified 1966 memo from the US nuclear program stated that uranium-233 has been shown to be highly satisfactory as a weapons material, though it was only superior to plutonium in rare circumstances. It was claimed that if the existing weapons were based on uranium-233 instead of plutonium-239, Livermore would not be interested in switching to plutonium.
The co-presence of uranium-232 can complicate the manufacture and use of uranium-233, though the Livermore memo indicates a likelihood that this complication can be worked around. aside, there is scant publicly available information on this isotope actually having been weaponized:
- The United States detonated an experimental device in the 1955 Operation Teapot "MET" test which used a plutonium/<sup>233</sup>U composite pit; its design was based on the plutonium/<sup>235</sup>U pit from the TX-7E, a prototype Mark 7 nuclear bomb design used in the 1951 Operation Buster-Jangle "Easy" test. Although not an outright fizzle, MET's actual yield of 22 kilotons was sufficiently below the predicted 33 kt that the information gathered was of limited value.
- The Soviet Union detonated its first hydrogen bomb the same year, the RDS-37, which contained a fissile core of <sup>235</sup>U and <sup>233</sup>U.
- In 1998, as part of its Pokhran-II tests, India detonated an experimental <sup>233</sup>U device of low-yield (0.2 kt) called Shakti V.
The B Reactor and others at the Hanford Site optimized for the production of weapons-grade material have been used to manufacture <sup>233</sup>U.
Overall the United States is thought to have produced two tons of <sup>233</sup>U, of various levels of purity, some with <sup>232</sup>U impurity content as low as 6 ppm.
The hazards are significant even at 5 parts per million. Implosion nuclear weapons require <sup>232</sup>U levels below 50 ppm (above which the <sup>233</sup>U is considered "low grade"; cf. "Standard weapon grade plutonium requires a <sup>240</sup>Pu content of no more than 6.5%." which is 65,000 ppm, and the analogous <sup>238</sup>Pu was produced in levels of 0.5% (5,000 ppm) or less). Gun-type fission weapons additionally need low levels (1 ppm range) of light impurities, to keep the neutron generation low.
The production of "clean" <sup>233</sup>U, low in <sup>232</sup>U, requires a few factors: 1) obtaining a relatively pure <sup>232</sup>Th source, low in <sup>230</sup>Th (which also transmutes to <sup>232</sup>U), 2) moderating the incident neutrons to have an energy not higher that 6 MeV (too-high energy neutrons cause the <sup>232</sup>Th (n,2n) → <sup>231</sup>Th reaction) and 3) removing the thorium sample from neutron flux before the <sup>233</sup>U concentration builds up to a too high level, in order to avoid fissioning the <sup>233</sup>U itself (which would produce energetic neutrons).
The Molten-Salt Reactor Experiment (MSRE) used <sup>233</sup>U, bred in light water reactors such as Indian Point Energy Center, that was about 220 ppm <sup>232</sup>U.
Further information
Thorium, from which <sup>233</sup>U is bred, is roughly three to four times more abundant in the Earth's crust than uranium.
The decay chain of <sup>233</sup>U itself is part of the neptunium series, the decay chain of its grandparent <sup>237</sup>Np.
Uses for uranium-233 include the production of the medical isotopes actinium-225 and bismuth-213 which are among its daughters, low-mass nuclear reactors for space travel applications, use as an isotopic tracer, nuclear weapons research, and reactor fuel research including the thorium fuel cycle.
