Uranium-233 is produced by the neutronirradiation of thorium-232. When thorium-232 absorbs a neutron, it becomes thorium-233, which has a half-life of only 22minutes. Thorium-233 decays into protactinium-233 through beta decay. Protactinium-233 has a half-life of 27days and beta decays into uranium-233; some proposed molten salt reactor designs attempt to physically isolate the protactinium from further neutron capture before beta decay can occur, to maintain the neutron economy (if it misses the 233U window, the next fissile target is 235U, meaning a total of 4 neutrons needed to trigger fission).
233U usually fissions on neutron absorption, but sometimes retains the neutron, becoming uranium-234. For both thermal neutrons and fast neutrons, the capture-to-fission ratio of uranium-233 is smaller than those of the other two major fissile fuels, uranium-235 and plutonium-239.[3]
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.[4][5]
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.[2] These were produced at the Hanford Site and Savannah River Site in reactors that were designed for the production of plutonium-239.[6]
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 = 3.171·10−11 J (i.e. 19.09TJ/mol = 81.95 TJ/kg = 22764 MWh/kg that is 1.8 million times more than the same mass of diesel).[7]
Source
Average energy released (MeV)
Instantaneously released energy
Kinetic energy of fission fragments
168.2
Kinetic energy of prompt neutrons
004.8
Energy carried by prompt γ-rays
007.7
Energy from decaying fission products
Energy of β− particles
005.2
Energy of anti-neutrinos
006.9
Energy of delayed γ-rays
005.0
Sum(excluding escaping anti-neutrinos)
191.0
Energy released when those prompt neutrons which don't (re)produce fission are captured
009.1
Energy converted into heat in an operating thermal nuclear reactor
200.1
Weapon material
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 4–5kg in beryllium-reflected sphere).[8] 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.[9]
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.[10]
The co-presence of uranium-232[11] can complicate the manufacture and use of uranium-233, though the Livermore memo indicates a likelihood that this complication can be worked around.[10]
While it is thus possible to use uranium-233 as the fissile material of a nuclear weapon, speculation[12] 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/233U composite pit; its design was based on the plutonium/235U 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.[13][14]
Overall the United States is thought to have produced two tons of 233U, of various levels of purity, some with 232U impurity content as low as 6ppm.[22]
232U impurity
Production of 233U (through the irradiation of thorium-232) invariably produces small amounts of uranium-232 as an impurity, because of parasitic (n,2n) reactions on uranium-233 itself, or on protactinium-233, or on thorium-232:
Another channel involves neutron capture reaction on small amounts of thorium-230, which is a tiny fraction of natural thorium present due to the decay of uranium-238:
The decay chain of 232U quickly yields strong gamma radiation emitters. Thallium-208 is the strongest of these, at 2.6MeV:
232U (α, 68.9 y)
228Th (α, 1.9 y)
224Ra (α, 5.44 MeV, 3.6 d, with a γ of 0.24 MeV)
220Rn (α, 6.29 MeV, 56 s, with a γ of 0.54 MeV)
216Po (α, 0.15 s)
212Pb (β−, 10.64 h)
212Bi (α, 61 min, 0.78 MeV)
208Tl (β−, 1.8 MeV, 3 min, with a γ of 2.6 MeV)
208Pb (stable)
This makes manual handling in a glove box with only light shielding (as commonly done with plutonium) too hazardous, (except possibly in a short period immediately following chemical separation of the uranium from its decay products) and instead requiring complex remote manipulation for fuel fabrication.
The hazards are significant even at 5 parts per million. Implosion nuclear weapons require 232U levels below 50ppm (above which the 233U is considered "low grade"; cf. "Standard weapon grade plutonium requires a 240Pu content of no more than 6.5%." which is 65,000ppm, and the analogous 238Pu was produced in levels of 0.5% (5,000ppm) or less). Gun-type fission weapons additionally need low levels (1ppm range) of light impurities, to keep the neutron generation low.[11][23]
The production of "clean" 233U, low in 232U, requires a few factors: 1) obtaining a relatively pure 232Th source, low in 230Th (which also transmutes to 232U), 2) moderating the incident neutrons to have an energy not higher that 6MeV (too-high energy neutrons cause the 232Th (n,2n) → 231Th reaction) and 3) removing the thorium sample from neutron flux before the 233U concentration builds up to a too high level, in order to avoid fissioning the 233U itself (which would produce energetic neutrons).[22][24]
Thorium, from which 233U is bred, is roughly three to four times more abundant in the Earth's crust than uranium.[26][27] The decay chain of 233U itself is part of the neptunium series, the decay chain of its grandparent 237Np.
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.[2]
↑ Nuclear proliferation factbook. Committee on Governmental Affairs. Subcommittee on Energy, N. Proliferation., United States. Congress. House. Committee on Foreign Affairs. Subcommittee on International Economic Policy and Trade., United States. Congress. House. Committee on Foreign Affairs. Subcommittee on Arms Control, I. Security. 1985. p.295. Retrieved 29 November 2019.
↑ Hansen, Chuck (2007). Swords of Armageddon: US Nuclear Weapons Development since 1945, Version 2. Chuckelea Publications. pp.I-262, I-270.
1 2 Langford, R. Everett (2004). Introduction to Weapons of Mass Destruction: Radiological, Chemical, and Biological. Hoboken, New Jersey: John Wiley & Sons. p.85. ISBN0471465607. "The US tested a few uranium-233 bombs, but the presence of uranium-232 in the uranium-233 was a problem; the uranium-232 is a copious alpha emitter and tended to 'poison' the uranium-233 bomb by knocking stray neutrons from impurities in the bomb material, leading to possible pre-detonation. Separation of the uranium-232 from the uranium-233 proved to be very difficult and not practical. The uranium-233 bomb was never deployed since plutonium-239 was becoming plentiful."
The actinide or actinoid series encompasses at least the 14 metallic chemical elements in the 5f series, with atomic numbers from 89 to 102, actinium through nobelium. The actinide series derives its name from the first element in the series, actinium. The informal chemical symbol An is used in general discussions of actinide chemistry to refer to any actinide.
Protactinium is a chemical element; it has symbol Pa and atomic number 91. It is a dense, radioactive, silvery-gray actinide metal which readily reacts with oxygen, water vapor, and inorganic acids. It forms various chemical compounds, in which protactinium is usually present in the oxidation state +5, but it can also assume +4 and even +3 or +2 states. Concentrations of protactinium in the Earth's crust are typically a few parts per trillion, but may reach up to a few parts per million in some uraninite ore deposits. Because of its scarcity, high radioactivity, and high toxicity, there are currently no uses for protactinium outside scientific research, and for this purpose, protactinium is mostly extracted from spent nuclear fuel.
Thorium is a chemical element. It has the symbol Th and atomic number 90. Thorium is a weakly radioactive light silver metal which tarnishes olive gray when it is exposed to air, forming thorium dioxide; it is moderately soft and malleable and has a high melting point. Thorium is an electropositive actinide whose chemistry is dominated by the +4 oxidation state; it is quite reactive and can ignite in air when finely divided.
In nuclear engineering, fissile material is material that can undergo nuclear fission when struck by a neutron of low energy. A self-sustaining thermal chain reaction can only be achieved with fissile material. The predominant neutron energy in a system may be typified by either slow neutrons or fast neutrons. Fissile material can be used to fuel thermal-neutron reactors, fast-neutron reactors and nuclear explosives.
The nuclear fuel cycle, also called nuclear fuel chain, is the progression of nuclear fuel through a series of differing stages. It consists of steps in the front end, which are the preparation of the fuel, steps in the service period in which the fuel is used during reactor operation, and steps in the back end, which are necessary to safely manage, contain, and either reprocess or dispose of spent nuclear fuel. If spent fuel is not reprocessed, the fuel cycle is referred to as an open fuel cycle ; if the spent fuel is reprocessed, it is referred to as a closed fuel cycle.
A breeder reactor is a nuclear reactor that generates more fissile material than it consumes. These reactors can be fueled with more-commonly available isotopes of uranium and thorium, such as uranium-238 and thorium-232, as opposed to the rare uranium-235 which is used in conventional reactors. These materials are called fertile materials since they can be bred into fuel by these breeder reactors.
Uranium-238 is the most common isotope of uranium found in nature, with a relative abundance of 99%. Unlike uranium-235, it is non-fissile, which means it cannot sustain a chain reaction in a thermal-neutron reactor. However, it is fissionable by fast neutrons, and is fertile, meaning it can be transmuted to fissile plutonium-239. 238U cannot support a chain reaction because inelastic scattering reduces neutron energy below the range where fast fission of one or more next-generation nuclei is probable. Doppler broadening of 238U's neutron absorption resonances, increasing absorption as fuel temperature increases, is also an essential negative feedback mechanism for reactor control.
Uranium-234 is an isotope of uranium. In natural uranium and in uranium ore, 234U occurs as an indirect decay product of uranium-238, but it makes up only 0.0055% of the raw uranium because its half-life of just 245,500 years is only about 1/18,000 as long as that of 238U. Thus the ratio of 234 U to 238 U in a natural sample is equivalent to the ratio of their half-lives. The primary path of production of 234U via nuclear decay is as follows: uranium-238 nuclei emit an alpha particle to become thorium-234. Next, with a short half-life, 234Th nuclei emit a beta particle to become protactinium-234 (234Pa), or more likely a nuclear isomer denoted 234mPa. Finally, 234Pa or 234mPa nuclei emit another beta particle to become 234U nuclei.
Fertile material is a material that, although not fissile itself, can be converted into a fissile material by neutron absorption.
Uranium (92U) is a naturally occurring radioactive element (radioelement) with no stable isotopes. It has two primordial isotopes, uranium-238 and uranium-235, that have long half-lives and are found in appreciable quantity in Earth's crust. The decay product uranium-234 is also found. Other isotopes such as uranium-233 have been produced in breeder reactors. In addition to isotopes found in nature or nuclear reactors, many isotopes with far shorter half-lives have been produced, ranging from 214U to 242U. The standard atomic weight of natural uranium is 238.02891(3).
Protactinium (91Pa) has no stable isotopes. The four naturally occurring isotopes allow a standard atomic weight to be given.
Neptunium (93Np) is usually considered an artificial element, although trace quantities are found in nature, so a standard atomic weight cannot be given. Like all trace or artificial elements, it has no stable isotopes. The first isotope to be synthesized and identified was 239Np in 1940, produced by bombarding 238 U with neutrons to produce 239 U , which then underwent beta decay to 239 Np .
Plutonium (94Pu) is an artificial element, except for trace quantities resulting from neutron capture by uranium, and thus a standard atomic weight cannot be given. Like all artificial elements, it has no stable isotopes. It was synthesized long before being found in nature, the first isotope synthesized being plutonium-238 in 1940. Twenty-one plutonium radioisotopes have been characterized. The most stable are plutonium-244 with a half-life of 80.8 million years; plutonium-242 with a half-life of 373,300 years; and plutonium-239 with a half-life of 24,110 years; and plutonium-240 with a half-life of 6,560 years. This element also has eight meta states; all have half-lives of less than one second.
The thorium fuel cycle is a nuclear fuel cycle that uses an isotope of thorium, 232 Th , as the fertile material. In the reactor, 232 Th is transmuted into the fissile artificial uranium isotope 233 U which is the nuclear fuel. Unlike natural uranium, natural thorium contains only trace amounts of fissile material, which are insufficient to initiate a nuclear chain reaction. Additional fissile material or another neutron source is necessary to initiate the fuel cycle. In a thorium-fuelled reactor, 232 Th absorbs neutrons to produce 233 U . This parallels the process in uranium breeder reactors whereby fertile 238 U absorbs neutrons to form fissile 239 Pu . Depending on the design of the reactor and fuel cycle, the generated 233 U either fissions in situ or is chemically separated from the used nuclear fuel and formed into new nuclear fuel.
Spent nuclear fuel, occasionally called used nuclear fuel, is nuclear fuel that has been irradiated in a nuclear reactor. It is no longer useful in sustaining a nuclear reaction in an ordinary thermal reactor and, depending on its point along the nuclear fuel cycle, it will have different isotopic constituents than when it started.
Weapons-grade nuclear material is any fissionable nuclear material that is pure enough to make a nuclear weapon and has properties that make it particularly suitable for nuclear weapons use. Plutonium and uranium in grades normally used in nuclear weapons are the most common examples.
Uranium-232 is an isotope of uranium. It has a half-life of around 69 years and is a side product in the thorium cycle. It has been cited as an obstacle to nuclear proliferation using 233U as the fissile material, because the intense gamma radiation emitted by 208Tl makes the 233U contaminated with it more difficult to handle.
Uranium-236 is an isotope of uranium that is neither fissile with thermal neutrons, nor very good fertile material, but is generally considered a nuisance and long-lived radioactive waste. It is found in spent nuclear fuel and in the reprocessed uranium made from spent nuclear fuel.
The liquid fluoride thorium reactor is a type of molten salt reactor. LFTRs use the thorium fuel cycle with a fluoride-based molten (liquid) salt for fuel. In a typical design, the liquid is pumped between a critical core and an external heat exchanger where the heat is transferred to a nonradioactive secondary salt. The secondary salt then transfers its heat to a steam turbine or closed-cycle gas turbine.
Nuclear transmutation is the conversion of one chemical element or an isotope into another chemical element. Nuclear transmutation occurs in any process where the number of protons or neutrons in the nucleus of an atom is changed.
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