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Nuclear Transmutation

plutonium breedingIn physics, nuclear transmutation is the conversion of one chemical element or an isotope into another. In nuclear engineering, also nuclear reactors cause artificial transmutation by exposing elements to neutrons produced by fission. In nuclear reactors, the most important phenomenon is the transmutation of fertile isotopes (e.g., uranium 238) into fissile isotopes (e.g., plutonium 239). The process of the transmutation of fertile materials to fissile materials is referred to as fuel breeding.

See also: Nuclear Breeding

Fertile materials are not capable of undergoing fission reaction after absorbing thermal (slow or low energyneutrons, and these materials are not capable of sustaining a nuclear fission chain reaction. There are two basic fertile materials: 238U and 232Th.

233U breeding:

n+_{90}^{232}\textrm{Th} {\rightarrow} _{90}^{232}\textrm{Th}+\gamma \rightarrow _{91}^{233}\textrm{Pa} \rightarrow _{92}^{233}\textrm{U}

232Th is the predominant isotope of natural thorium. If this fertile material is loaded in the nuclear reactor, the nuclei of 232Th absorb a neutron and become nuclei of 233Th. The half-life of 233Th is approximately 21.8 minutes. 233Th decays (negative beta decay) to 233Pa (protactinium), whose half-life is 26.97 days. 233Pa decays (negative beta decay)  to 233U, which is a very good fissile material. On the other hand, proposed reactor designs must attempt to physically isolate the protactinium from further neutron capture before beta decay can occur.

239Pu breeding:

 n+_{92}^{238}\textrm{U} {\rightarrow} _{92}^{239}\textrm{U}+\gamma \rightarrow _{93}^{239}\textrm{Np} \rightarrow _{94}^{239}\textrm{Pu} 

Neutron capture may also be used to create fissile 239Pu from 238U, the dominant constituent of naturally occurring uranium (99.28%). Absorption of a neutron in the 238U nucleus yields 239U. The half-life of 239U is approximately 23.5 minutes. 239decays (negative beta decay) to 239Np (neptunium), whose half-life is 2.36 days. 239Np decays (negative beta decay)  to 239Pu.

Transmutation of transuranium elements (i.e., the chemical elements with atomic numbers greater than 92 ) such as the isotopes of plutonium has the potential to help solve some problems posed by the management of radioactive waste by reducing the proportion of long-lived isotopes it contains.

californium-252 as a neutron source
Scheme of the production of californium-252 from uranium-238 by neutron irradiation.
Source: wikipedia.org

Fuel Depletion – Isotopic Changes

Fuel Depletion - Isotopic Changes
Isotopic changes of 4% uranium-235 fuel as a function of fuel burnup.

As a reactor is operated at significant power, fuel atoms are constantly consumed, resulting in the slow depletion of the fuel. It must be noted there are also research reactors, which have very low power, and the fuel in these reactors does not change its isotopic composition.

Research reactors with significant thermal power and all power reactors are subjected to significant isotopic changes. The study of these isotopic changes is known as long-term kinetics, which describes phenomena that occur over months or even years. The study of phenomena that occur for several hours to a few days, for example, effects of neutron poisons on the reactivity (i.e., Xenon poisoning or spatial oscillations), is known as medium-term kinetics.
This chapter describes the long-term kinetics of thermal reactors based on the uranium fuel cycle, in which a fuel with a large concentration of uranium-238 is used (e.g., PWRs or BWRs). Most common reactor fuels are composed of either natural or partially enriched uranium. Typically, PWRs use an enriched uranium fuel (~4% of U-235) as a fresh fuel. Exposure to neutron flux gradually depletes the uranium-235, decreasing core reactivity (compensated by control rods, chemical shim, or burnable absorbers). The initial fuel load of a new reactor core (so-called first core) is entirely fresh fuel, fuel with no plutonium or fission products present. The contribution of uranium-238 directly to fission is quite small in most thermal reactors. On the other hand, uranium-238 plays a very important role, and this chapter is primarily about this isotope.

See also: Uranium

See also: Plutonium

 
Uranium 235
Fissile / Fertile Material Cross-sections
Source: JANIS (Java-based nuclear information software)
http://www.oecd-nea.org/janis/

is a fissile isotope and its fission cross-section for thermal neutrons is about 585 barns (for 0.0253 eV neutron). For fast neutrons its fission cross-section is on the order of barns. Most of absorption reactions result in fission reaction, but a minority results in radiative capture forming 236U. The cross-section for radiative capture for thermal neutrons is about 99 barns (for 0.0253 eV neutron). Therefore about 15% of all absorption reactions result in radiative capture of neutron. About 85% of all absorption reactions result in fission.

Uranium absorption reaction

Uranium 238
Fissile / Fertile Material Cross-sections
Fissile / Fertile Material Cross-sections. Uranium 238.
Source: JANIS (Java-based nuclear information software)
http://www.oecd-nea.org/janis/

238U is a fissionable isotope but is not a fissile isotope. 238U is not capable of undergoing a fission reaction after absorbing a thermal neutron. On the other hand, 238U can be fissioned by fast neutron with energy higher than >1MeV. During the fuel burning, the content of the U-235 continuously decreases, and the content of the plutonium increases (up to ~1% of Pu ). 238U also belongs to the group of fertile isotopes. Radiative capture of a neutron leads to the formation of fissile 239Pu and other transuranic elements. This is the way how 238U contributes to the operation of nuclear reactors and the production of electricity through this plutonium. For example, at a burnup of 40GWd/tU, about 40% of the total energy released comes from bred plutonium. This corresponds to a breeding ratio for this fuel burnup of about 0.4 to 0.5. That means about half of the fissile fuel in these reactors is bred there. This effect extends the cycle length for such fuels to sometimes nearly twice what it would otherwise be. MOX fuel has a smaller breeding effect than 235U fuel and is thus more challenging and slightly less economical to use due to a quicker drop-off in reactivity through cycle life.

Equation - Plutonium 239 breeding from Uranium 238

Plutonium 239
Fissile / Fertile Material Cross-sections
Source: JANIS (Java-based nuclear information software)
http://www.oecd-nea.org/janis/

Plutonium 239 is a fissile isotope, and its fission cross-section for thermal neutrons is about 750 barns (for 0.025 eV neutron). For fast neutrons, its fission cross-section is on the order of barns. Most absorption reactions result in fission reactions, but a part of reactions result in radiative capture forming 240Pu. The cross-section for radiative capture for thermal neutrons is about 270 barns (for 0.025 eV neutron). Therefore about 27% of all absorption reactions result in radiative capture of incident neutron. About 73% of all absorption reactions result in fission.

Plutonium fission vs. radiative capture

Plutonium 241
Fissile / Fertile Material Cross-sections
Source: JANIS (Java-based nuclear information software)
http://www.oecd-nea.org/janis/

241Pu is a fissile isotope, which means 241Pu is capable of undergoing fission reaction after absorbing thermal neutron. Moreover 241Pu meets also alternative requirement that the amount of neutrons produced by fission of 241Pu (~2.94 per one fission by thermal neutron) is sufficient to sustain a nuclear fission chain reaction. Its fission cross-section for thermal neutrons is about 1012 barns (for 0.025 eV neutron). For fast neutrons its fission cross-section is on the order of barns. Most of absorption reactions result in fission reaction, but a part of reactions result in radiative capture forming 242Pu. The cross-section for radiative capture for thermal neutrons is about 363 barns (for 0.025 eV neutron). Therefore about 74% of all absorption reactions result in radiative capture of neutron. About 26% of all absorption reactions result in fission. 241Pu decays via beta decay into 241Am with half-life of only 14.3 years. 241Am has relatively high cross-section for radiative capture for thermal neutrons (~680 barns – 0.025eV). This two phenomena (decrease in fissile isotope and increase in neutron absorber) cause slight decrease in reactivity of irradiated fuel when stored in a spent fuel pool.

Evolution Equations

The exact evolution of isotopic changes is usually modeled mathematically by a set of differential equations known as evolution equations. These equations describe the rate of burnup of U-235, the rate of buildup of Pu-239, production of Pu-240 and Pu-241, the buildup of neutron-absorbing fission products and the overall rate of reactivity change in the reactor due to the changing composition of the fuel. The evolution equation can be constructed for each isotope. For example:

Evolution Equations

Special reference: W. M. Stacey, Nuclear Reactor Physics, John Wiley & Sons, 2001, ISBN: 0- 471-39127-1.

Special reference: Paul Reuss, Neutron Physics, EDP Sciences, 2008, ISBN: 2759800415.

Isotopic Changes – Summary

Fuel Depletion - Isotopic Changes
Isotopic changes of 4% uranium-235 fuel as a function of fuel burnup.

In summary, it can be seen for fuel burnup of 40 GWd/tU:

  • Approximately 3 – 4% of the heavy nuclei are fissioned.
  • About two-thirds of these fissions come directly from uranium 235, and the other third comes from plutonium produced from uranium 238. The contribution significantly increases as the fuel burnup increases.
  • The removed fuel (spent nuclear fuel) still contains about 96% reusable material. It must be removed due to decreasing kinf of an assembly, or in other words, it must be removed due to accumulation of fission products with significant absorption cross-section.
  • Discharged fuel contains about 0.8% of plutonium and about 1% of uranium 235. It must be noted there is a significant content (about 0.5%) of uranium 236, which is neither a fissile isotope nor a fertile isotope.
 
References:
Nuclear and Reactor Physics:
  1. J. R. Lamarsh, Introduction to Nuclear Reactor Theory, 2nd ed., Addison-Wesley, Reading, MA (1983).
  2. J. R. Lamarsh, A. J. Baratta, Introduction to Nuclear Engineering, 3d ed., Prentice-Hall, 2001, ISBN: 0-201-82498-1.
  3. W. M. Stacey, Nuclear Reactor Physics, John Wiley & Sons, 2001, ISBN: 0- 471-39127-1.
  4. Glasstone, Sesonske. Nuclear Reactor Engineering: Reactor Systems Engineering, Springer; 4th edition, 1994, ISBN: 978-0412985317
  5. W.S.C. Williams. Nuclear and Particle Physics. Clarendon Press; 1 edition, 1991, ISBN: 978-0198520467
  6. G.R.Keepin. Physics of Nuclear Kinetics. Addison-Wesley Pub. Co; 1st edition, 1965
  7. Robert Reed Burn, Introduction to Nuclear Reactor Operation, 1988.
  8. U.S. Department of Energy, Nuclear Physics and Reactor Theory. DOE Fundamentals Handbook, Volume 1 and 2. January 1993.

Advanced Reactor Physics:

  1. K. O. Ott, W. A. Bezella, Introductory Nuclear Reactor Statics, American Nuclear Society, Revised edition (1989), 1989, ISBN: 0-894-48033-2.
  2. K. O. Ott, R. J. Neuhold, Introductory Nuclear Reactor Dynamics, American Nuclear Society, 1985, ISBN: 0-894-48029-4.
  3. D. L. Hetrick, Dynamics of Nuclear Reactors, American Nuclear Society, 1993, ISBN: 0-894-48453-2. 
  4. E. E. Lewis, W. F. Miller, Computational Methods of Neutron Transport, American Nuclear Society, 1993, ISBN: 0-894-48452-4.

See above:

Reactor Operation