Jump to content

Enriched uranium

From Wikipedia, the free encyclopedia
(Redirected from Uranium-enrichment)

Enriched uranium is a type of uranium in which the percent composition of uranium-235 (written 235U) has been increased through the process of isotope separation. Naturally occurring uranium is composed of three major isotopes: uranium-238 (238U with 99.2732–99.2752% natural abundance), uranium-235 (235U, 0.7198–0.7210%), and uranium-234 (234U, 0.0049–0.0059%).[1] 235U is the only nuclide existing in nature (in any appreciable amount) that is fissile with thermal neutrons.[2]

Proportions of uranium-238 (blue) and uranium-235 (red) found naturally versus enriched grades

Enriched uranium is a critical component for both civil nuclear power generation and military nuclear weapons.

There are about 2,000 tonnes of highly enriched uranium in the world,[3] produced mostly for nuclear power, nuclear weapons, naval propulsion, and smaller quantities for research reactors.

The 238U remaining after enrichment is known as depleted uranium (DU), and is considerably less radioactive than even natural uranium, though still very dense. Depleted uranium is used as a radiation shielding material and for armor-penetrating weapons.

Grades

[edit]

Uranium as it is taken directly from the Earth is not suitable as fuel for most nuclear reactors and requires additional processes to make it usable (CANDU design is a notable exception). Uranium is mined either underground or in an open pit depending on the depth at which it is found. After the uranium ore is mined, it must go through a milling process to extract the uranium from the ore.

This is accomplished by a combination of chemical processes with the end product being concentrated uranium oxide, which is known as "yellowcake", contains roughly 80% uranium whereas the original ore typically contains as little as 0.1% uranium.[4]

This yellowcake is further processed to obtain the desired form of uranium suitable for nuclear fuel production. After the milling process is complete, the uranium must next undergo a process of conversion, "to either uranium dioxide, which can be used as the fuel for those types of reactors that do not require enriched uranium, or into uranium hexafluoride, which can be enriched to produce fuel for the majority of types of reactors".[5] Naturally occurring uranium is made of a mixture of 235U and 238U. The 235U is fissile, meaning it is easily split with neutrons while the remainder is 238U, but in nature, more than 99% of the extracted ore is 238U. Most nuclear reactors require enriched uranium, which is uranium with higher concentrations of 235U ranging between 3.5% and 4.5% (although a few reactor designs using a graphite or heavy water moderator, such as the RBMK and CANDU, are capable of operating with natural uranium as fuel). There are two commercial enrichment processes: gaseous diffusion and gas centrifugation. Both enrichment processes involve the use of uranium hexafluoride and produce enriched uranium oxide.[6]

A drum of yellowcake (a mixture of uranium precipitates)

Reprocessed uranium (RepU)

[edit]
Main article: Reprocessed uranium

Reprocessed uranium (RepU) undergoes a series of chemical and physical treatments to extract usable uranium from spent nuclear fuel. RepU is a product of nuclear fuel cycles involving nuclear reprocessing of spent fuel. RepU recovered from light water reactor (LWR) spent fuel typically contains slightly more 235U than natural uranium, and therefore could be used to fuel reactors that customarily use natural uranium as fuel, such as CANDU reactors. It also contains the undesirable isotope uranium-236, which undergoes neutron capture, wasting neutrons (and requiring higher 235U enrichment) and creating neptunium-237, which would be one of the more mobile and troublesome radionuclides in deep geological repository disposal of nuclear waste. Reprocessed uranium often carries traces of other transuranic elements and fission products, necessitating careful monitoring and management during fuel fabrication and reactor operation.

Low-enriched uranium (LEU)

[edit]

Low-enriched uranium (LEU) has a lower than 20% concentration of 235U; for instance, in commercial LWR, the most prevalent power reactors in the world, uranium is enriched to 3 to 5% 235U. Slightly enriched uranium (SEU) has a concentration of under 2% 235U.[7]

High-assay LEU (HALEU)

[edit]

High-assay LEU (HALEU) is enriched between 5% and 20%[8] and is called for in many small modular reactor (SMR) designs.[9] Fresh LEU used in research reactors is usually enriched between 12% and 19.75% 235U; the latter concentration is used to replace HEU fuels when converting to LEU.[10]

Highly enriched uranium (HEU)

[edit]
A billet of highly enriched uranium metal

Highly enriched uranium (HEU) has a 20% or higher concentration of 235U. This high enrichment level is essential for nuclear weapons and certain specialized reactor designs. The fissile uranium in nuclear weapon primaries usually contains 85% or more of 235U known as weapons grade, though theoretically for an implosion design, a minimum of 20% could be sufficient (called weapon-usable) although it would require hundreds of kilograms of material and "would not be practical to design";[11][12] even lower enrichment is hypothetically possible, but as the enrichment percentage decreases the critical mass for unmoderated fast neutrons rapidly increases, with for example, an infinite mass of 5.4% 235U being required.[11] For criticality experiments, enrichment of uranium to over 97% has been accomplished.[13]

The first uranium bomb, Little Boy, dropped by the United States on Hiroshima in 1945, used 64 kilograms (141 lb) of 80% enriched uranium. Wrapping the weapon's fissile core in a neutron reflector (which is standard on all nuclear explosives) can dramatically reduce the critical mass. Because the core was surrounded by a good neutron reflector, at explosion it comprised almost 2.5 critical masses. Neutron reflectors, compressing the fissile core via implosion, fusion boosting, and "tamping", which slows the expansion of the fissioning core with inertia, allow nuclear weapon designs that use less than what would be one bare-sphere critical mass at normal density. The presence of too much of the 238U isotope inhibits the runaway nuclear chain reaction that is responsible for the weapon's power. The critical mass for 85% highly enriched uranium is about 50 kilograms (110 lb), which at normal density would be a sphere about 17 centimetres (6.7 in) in diameter.[14]

Later U.S. nuclear weapons usually use plutonium-239 in the primary stage, but the jacket or tamper secondary stage, which is compressed by the primary nuclear explosion often uses HEU with enrichment between 40% and 80%[15] along with the fusion fuel lithium deuteride. This multi-stage design enhances the efficiency and effectiveness of nuclear weapons, allowing for greater control over the release of energy during detonation. For the secondary of a large nuclear weapon, the higher critical mass of less-enriched uranium can be an advantage as it allows the core at explosion time to contain a larger amount of fuel. This design strategy optimizes the explosive yield and performance of advanced nuclear weapons systems. The 238U is not said to be fissile but still is fissionable by fast neutrons (>2 MeV) such as the ones produced during D–T fusion.[16]

HEU is also used in fast neutron reactors, whose cores require about 20% or more of fissile material, as well as in naval reactors, where it often contains at least 50% 235U, but typically does not exceed 90%. These specialized reactor systems rely on highly enriched uranium for their unique operational requirements, including high neutron flux and precise control over reactor dynamics. The Fermi-1 commercial fast reactor prototype used HEU with 26.5% 235U. Significant quantities of HEU are used in the production of medical isotopes, for example molybdenum-99 for technetium-99m generators.[17]The medical industry benefits from the unique properties of highly enriched uranium, which enable the efficient production of critical isotopes essential for diagnostic imaging and therapeutic applications

Enrichment methods

[edit]

Isotope separation is difficult because two isotopes of the same element have nearly identical chemical properties, and can only be separated gradually using small mass differences. (235U is only 1.26% lighter than 238U.) This problem is compounded because uranium is rarely separated in its atomic form, but instead as a compound (235UF6 is only 0.852% lighter than 238UF6). A cascade of identical stages produces successively higher concentrations of 235U. Each stage passes a slightly more concentrated product to the next stage and returns a slightly less concentrated residue to the previous stage.

There are currently two generic commercial methods employed internationally for enrichment: gaseous diffusion (referred to as first generation) and gas centrifuge (second generation), which consumes only 2% to 2.5%[18] as much energy as gaseous diffusion. Some work is being done that would use nuclear resonance; however, there is no reliable evidence that any nuclear resonance processes have been scaled up to production.

Diffusion techniques

[edit]

Gaseous diffusion

[edit]
Main article: Gaseous diffusion
Gaseous diffusion uses semi-permeable membranes to separate enriched uranium.

Gaseous diffusion is a technology used to produce enriched uranium by forcing gaseous uranium hexafluoride (hex) through semi-permeable membranes. This produces a slight separation between the molecules containing 235U and 238U. Throughout the Cold War, gaseous diffusion played a major role as a uranium enrichment technique, and as of 2008 accounted for about 33% of enriched uranium production,[19] but in 2011 was deemed an obsolete technology that is steadily being replaced by the later generations of technology as the diffusion plants reach their ends of life.[20] In 2013, the Paducah facility in the U.S. ceased operating, it was the last commercial 235U gaseous diffusion plant in the world.[21]

Thermal diffusion

[edit]

Thermal diffusion uses the transfer of heat across a thin liquid or gas to accomplish isotope separation.[22] The process exploits the fact that the lighter 235U gas molecules will diffuse toward a hot surface, and the heavier 238U gas molecules will diffuse toward a cold surface. The S-50 plant at Oak Ridge, Tennessee, was used during World War II to prepare feed material for the Electromagnetic isotope separation (EMIS) process, explained later in this article. It was abandoned in favor of gaseous diffusion.

Centrifuge techniques

[edit]

Gas centrifuge

[edit]
Main article: Gas centrifuge
A cascade of gas centrifuges at a U.S. enrichment plant

The gas centrifuge process uses a large number of rotating cylinders in series and parallel formations. Each cylinder's rotation creates a strong centripetal force so that the heavier gas molecules containing 238U move tangentially toward the outside of the cylinder and the lighter gas molecules rich in 235U collect closer to the center. It requires much less energy to achieve the same separation than the older gaseous diffusion process, which it has largely replaced and so is the current method of choice and is termed second generation. It has a separation factor per stage of 1.3 relative to gaseous diffusion of 1.005,[19] which translates to about one-fiftieth of the energy requirements. Gas centrifuge techniques produce close to 100% of the world's enriched uranium. The cost per separative work unit is approximately 100 dollars per Separative Work Units (SWU), making it about 40% cheaper than standard gaseous diffusion techniques.[23]

Zippe centrifuge

[edit]
Main article: Zippe-type centrifuge
Diagram of the principles of a Zippe-type gas centrifuge with U-238 represented in dark blue and U-235 represented in light blue

The Zippe-type centrifuge is an improvement on the standard gas centrifuge, the primary difference being the use of heat. The bottom of the rotating cylinder is heated, producing convection currents that move the 235U up the cylinder, where it can be collected by scoops. This improved centrifuge design is used commercially by Urenco to produce nuclear fuel and was used by Pakistan in their nuclear weapons program.

Laser techniques

[edit]

Laser processes promise lower energy inputs, lower capital costs and lower tails assays, hence significant economic advantages. Several laser processes have been investigated or are under development. Separation of isotopes by laser excitation (SILEX) is well developed and is licensed for commercial operation as of 2012. Separation of isotopes by laser excitation is a very effective and cheap method of uranium separation, able to be done in small facilities requiring much less energy and space than previous separation techniques. The cost of uranium enrichment using laser enrichment technologies is approximately $30 per SWU[23] which is less than a third of the price of gas centrifuges, the current standard of enrichment. Separation of isotopes by laser excitation could be done in facilities virtually undetectable by satellites.[24] More than 20 countries have worked with laser separation over the past two decades, the most notable of these countries being Iran and North Korea, though all countries have had very limited success up to this point.

Atomic vapor laser isotope separation (AVLIS)

[edit]

Atomic vapor laser isotope separation employs specially tuned lasers[25] to separate isotopes of uranium using selective ionization of hyperfine transitions. The technique uses lasers tuned to frequencies that ionize 235U atoms and no others. The positively charged 235U ions are then attracted to a negatively charged plate and collected.

Molecular laser isotope separation (MLIS)

[edit]

Molecular laser isotope separation uses an infrared laser directed at UF6, exciting molecules that contain a 235U atom. A second laser frees a fluorine atom, leaving uranium pentafluoride, which then precipitates out of the gas.

Separation of isotopes by laser excitation (SILEX)

[edit]

Separation of isotopes by laser excitation is an Australian development that also uses UF6. After a protracted development process involving U.S. enrichment company USEC acquiring and then relinquishing commercialization rights to the technology, GE Hitachi Nuclear Energy (GEH) signed a commercialization agreement with Silex Systems in 2006.[26] GEH has since built a demonstration test loop and announced plans to build an initial commercial facility.[27] Details of the process are classified and restricted by intergovernmental agreements between United States, Australia, and the commercial entities. SILEX has been projected to be an order of magnitude more efficient than existing production techniques but again, the exact figure is classified.[19] In August, 2011 Global Laser Enrichment, a subsidiary of GEH, applied to the U.S. Nuclear Regulatory Commission (NRC) for a permit to build a commercial plant.[28] In September 2012, the NRC issued a license for GEH to build and operate a commercial SILEX enrichment plant, although the company had not yet decided whether the project would be profitable enough to begin construction, and despite concerns that the technology could contribute to nuclear proliferation.[29] The fear of nuclear proliferation arose in part due to laser separation technology requiring less than 25% of the space of typical separation techniques, as well as requiring only the energy that would power 12 typical houses, putting a laser separation plant that works by means of laser excitation well below the detection threshold of existing surveillance technologies.[24] Due to these concerns the American Physical Society filed a petition with the NRC, asking that before any laser excitation plants are built that they undergo a formal review of proliferation risks. The APS even went as far as calling the technology a "game changer"[23] due to the ability for it to be hidden from any type of detection.

Other techniques

[edit]

Aerodynamic processes

[edit]
Schematic diagram of an aerodynamic nozzle. Many thousands of these small foils would be combined in an enrichment unit.
The X-ray-based LIGA manufacturing process was originally developed at the Forschungszentrum Karlsruhe, Germany, to produce nozzles for isotope enrichment.[30]

Aerodynamic enrichment processes include the Becker jet nozzle techniques developed by E. W. Becker and associates using the LIGA process and the vortex tube separation process. These aerodynamic separation processes depend upon diffusion driven by pressure gradients, as does the gas centrifuge. They in general have the disadvantage of requiring complex systems of cascading of individual separating elements to minimize energy consumption. In effect, aerodynamic processes can be considered as non-rotating centrifuges. Enhancement of the centrifugal forces is achieved by dilution of UF6 with hydrogen or helium as a carrier gas achieving a much higher flow velocity for the gas than could be obtained using pure uranium hexafluoride. The Uranium Enrichment Corporation of South Africa (UCOR) developed and deployed the continuous Helikon vortex separation cascade for high production rate low-enrichment and the substantially different semi-batch Pelsakon low production rate high enrichment cascade both using a particular vortex tube separator design, and both embodied in industrial plant.[31] A demonstration plant was built in Brazil by NUCLEI, a consortium led by Industrias Nucleares do Brasil that used the separation nozzle process. However, all methods have high energy consumption and substantial requirements for removal of waste heat; none is currently still in use.

Electromagnetic isotope separation

[edit]
Main article: Calutron
Schematic diagram of uranium isotope separation in a calutron shows how a strong magnetic field is used to redirect a stream of uranium ions to a target, resulting in a higher concentration of uranium-235 (represented here in dark blue) in the inner fringes of the stream.

In the electromagnetic isotope separation process (EMIS), metallic uranium is first vaporized, and then ionized to positively charged ions. The cations are then accelerated and subsequently deflected by magnetic fields onto their respective collection targets. A production-scale mass spectrometer named the Calutron was developed during World War II that provided some of the 235U used for the Little Boy nuclear bomb, which was dropped over Hiroshima in 1945. Properly the term 'Calutron' applies to a multistage device arranged in a large oval around a powerful electromagnet. Electromagnetic isotope separation has been largely abandoned in favour of more effective methods.

Chemical methods

[edit]

One chemical process has been demonstrated to pilot plant stage but not used for production. The French CHEMEX process exploited a very slight difference in the two isotopes' propensity to change valency in oxidation/reduction, using immiscible aqueous and organic phases. An ion-exchange process was developed by the Asahi Chemical Company in Japan that applies similar chemistry but effects separation on a proprietary resin ion-exchange column.

Plasma separation

[edit]

Plasma separation process (PSP) describes a technique that makes use of superconducting magnets and plasma physics. In this process, the principle of ion cyclotron resonance is used to selectively energize the 235U isotope in a plasma containing a mix of ions. France developed its own version of PSP, which it called RCI. Funding for RCI was drastically reduced in 1986, and the program was suspended around 1990, although RCI is still used for stable isotope separation.

Separative work unit

[edit]
Further information: Separative work units

"Separative work"—the amount of separation done by an enrichment process—is a function of the concentrations of the feedstock, the enriched output, and the depleted tailings; and is expressed in units that are so calculated as to be proportional to the total input (energy / machine operation time) and to the mass processed. Separative work is not energy. The same amount of separative work will require different amounts of energy depending on the efficiency of the separation technology.[22] Separative work is measured in Separative work units SWU, kg SW, or kg UTA (from the German Urantrennarbeit – literally uranium separation work). Efficient utilization of separative work is crucial for optimizing the economic and operational performance of uranium enrichment facilities.

  • 1 SWU = 1 kg SW = 1 kg UTA
  • 1 kSWU = 1 tSW = 1 t UTA
  • 1 MSWU = 1 ktSW = 1 kt UTA

Cost issues

[edit]

In addition to the separative work units provided by an enrichment facility, the other important parameter to be considered is the mass of natural uranium (NU) that is needed to yield a desired mass of enriched uranium. As with the number of SWUs, the amount of feed material required will also depend on the level of enrichment desired and upon the amount of 235U that ends up in the depleted uranium. However, unlike the number of SWUs required during enrichment, which increases with decreasing levels of 235U in the depleted stream, the amount of NU needed will decrease with decreasing levels of 235U that end up in the DU.

For example, in the enrichment of LEU for use in a light water reactor it is typical for the enriched stream to contain 3.6% 235U (as compared to 0.7% in NU) while the depleted stream contains 0.2% to 0.3% 235U. In order to produce one kilogram of this LEU it would require approximately 8 kilograms of NU and 4.5 SWU if the DU stream was allowed to have 0.3% 235U. On the other hand, if the depleted stream had only 0.2% 235U, then it would require just 6.7 kilograms of NU, but nearly 5.7 SWU of enrichment. Because the amount of NU required and the number of SWUs required during enrichment change in opposite directions, if NU is cheap and enrichment services are more expensive, then the operators will typically choose to allow more 235U to be left in the DU stream whereas if NU is more expensive and enrichment is less so, then they would choose the opposite.

When converting uranium (hexafluoride, hex for short) to metal, 0.3% is lost during manufacturing.[32][33]

Downblending

[edit]

The opposite of enriching is downblending; surplus HEU can be downblended to LEU to make it suitable for use in commercial nuclear fuel. Downblending is a key process in nuclear non-proliferation efforts, as it reduces the amount of highly enriched uranium available for potential weaponization while repurposing it for peaceful purposes.

Enriched uranium produced at LLNL plant was collected as nuggets the size and thickness of several quarters.

The HEU feedstock can contain unwanted uranium isotopes: 234U is a minor isotope contained in natural uranium (primarily as a product of alpha decay of 238
U—because the half-life of 238
U is much larger than that of 234
U, it is be produced and destroyed at the same rate in a constant steady state equilibrium, bringing any sample with sufficient 238
U content to a stable ratio of 234
U to 238
U over long enough timescales); during the enrichment process, its concentration increases but remains well below 1%. High concentrations of 236U are a byproduct from irradiation in a reactor and may be contained in the HEU, depending on its manufacturing history. 236
U is produced primarily when 235
U absorbs a neutron and does not fission. The production of 236
U is thus unavoidable in any thermal neutron reactor with 235
U fuel. HEU reprocessed from nuclear weapons material production reactors (with an 235U assay of approximately 50%) may contain 236U concentrations as high as 25%, resulting in concentrations of approximately 1.5% in the blended LEU product. 236U is a neutron poison; therefore the actual 235U concentration in the LEU product must be raised accordingly to compensate for the presence of 236U. While 234
U also absorbs neutrons, it is a fertile material that is turned into fissile 235
U upon neutron absorption. If 236
U absorbs a neutron, the resulting short-lived 237
U beta decays to 237
Np, which is not usable in thermal neutron reactors but can be chemically separated from spent fuel to be disposed of as waste or to be transmutated into 238
Pu (for use in nuclear batteries) in special reactors. Understanding and managing the isotopic composition of uranium during downblending processes is essential to ensure the quality and safety of the resulting nuclear fuel, as well as to mitigate potential radiological and proliferation risks associated with unwanted isotopes.

The blendstock can be NU or DU; however, depending on feedstock quality, SEU at typically 1.5 wt% 235U may be used as a blendstock to dilute the unwanted byproducts that may be contained in the HEU feed. Concentrations of these isotopes in the LEU product in some cases could exceed ASTM specifications for nuclear fuel if NU or DU were used. So, the HEU downblending generally cannot contribute to the waste management problem posed by the existing large stockpiles of depleted uranium. Effective management and disposition strategies for depleted uranium are crucial to ensure long-term safety and environmental protection. Innovative approaches such as reprocessing and recycling of depleted uranium could offer sustainable solutions to minimize waste and optimize resource utilization in the nuclear fuel cycle.

A major downblending undertaking called the Megatons to Megawatts Program converts ex-Soviet weapons-grade HEU to fuel for U.S. commercial power reactors. From 1995 through mid-2005, 250 tonnes of high-enriched uranium (enough for 10,000 warheads) was recycled into low-enriched uranium. The goal is to recycle 500 tonnes by 2013. The decommissioning programme of Russian nuclear warheads accounted for about 13% of total world requirement for enriched uranium leading up to 2008.[19]This ambitious initiative not only addresses nuclear disarmament goals but also serves as a significant contributor to global energy security and environmental sustainability, effectively repurposing material once intended for destructive purposes into a resource for peaceful energy production.

The United States Enrichment Corporation has been involved in the disposition of a portion of the 174.3 tonnes of highly enriched uranium (HEU) that the U.S. government declared as surplus military material in 1996. Through the U.S. HEU Downblending Program, this HEU material, taken primarily from dismantled U.S. nuclear warheads, was recycled into low-enriched uranium (LEU) fuel, used by nuclear power plants to generate electricity.[34][35]This innovative program not only facilitated the safe and secure elimination of excess weapons-grade uranium but also contributed to the sustainable operation of civilian nuclear power plants, reducing reliance on newly enriched uranium and promoting non-proliferation efforts globally

Global enrichment facilities

[edit]
See also: Georges-Besse plant

The following countries are known to operate enrichment facilities: Argentina, Brazil, China, France, Germany, India, Iran, Japan, the Netherlands, North Korea, Pakistan, Russia, the United Kingdom, and the United States.[36][37] Belgium, Iran, Italy, and Spain hold an investment interest in the French Eurodif enrichment plant, with Iran's holding entitling it to 10% of the enriched uranium output. Countries that had enrichment programs in the past include Libya and South Africa, although Libya's facility was never operational.[38] The Australian company Silex Systems has developed a laser enrichment process known as SILEX (separation of isotopes by laser excitation), which it intends to pursue through financial investment in a U.S. commercial venture by General Electric,[39] Although SILEX has been granted a license to build a plant, the development is still in its early stages as laser enrichment has yet to be proven to be economically viable, and there is a petition being filed to review the license given to SILEX over nuclear proliferation concerns.[40] It has also been claimed that Israel has a uranium enrichment program housed at the Negev Nuclear Research Center site near Dimona.[41]

Codename

[edit]

During the Manhattan Project, weapons-grade highly enriched uranium was given the codename oralloy, a shortened version of Oak Ridge alloy, after the location of the plants where the uranium was enriched.[42] This covert terminology underscores the secrecy and sensitivity surrounding the production of highly enriched uranium during World War II, highlighting the strategic importance of the Manhattan Project and its role in the development of nuclear weapons. The term oralloy is still occasionally used to refer to enriched uranium.

See also

[edit]

References

[edit]
  1. ^ Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3): 030001. doi:10.1088/1674-1137/abddae.
  2. ^ OECD Nuclear Energy Agency (2003). Nuclear Energy Today. OECD Publishing. p. 25. ISBN 9789264103283.
  3. ^ Cochran (Natural Resources Defense Council), Thomas B. (12 June 1997). "Safeguarding Nuclear Weapon-Usable Materials in Russia" (PDF). Proceedings of international forum on illegal nuclear traffic. Archived from the original (PDF) on 22 July 2012.
  4. ^ Nuclear Fuel Cycle Overview, Uranium milling. World Nuclear Association, update April 2021
  5. ^ "Radiological Sources of Potential Exposure and/or Contamination". U.S. Army Center for Health Promotion and Preventive Medicine. June 1999. p. 27. Retrieved 1 July 2019.
  6. ^ Olander, Donald R. (1 January 1981). "The theory of uranium enrichment by the gas centrifuge". Progress in Nuclear Energy. 8 (1): 1–33. doi:10.1016/0149-1970(81)90026-3. ISSN 0149-1970.
  7. ^ Carter, John P.; Borrelli, R.A. (August 2020). "Integral molten salt reactor neutron physics study using Monte Carlo N-particle code". Nuclear Engineering and Design. 365: 110718. doi:10.1016/j.nucengdes.2020.110718. S2CID 225435681.
  8. ^ Herczeg, John W. (28 March 2019). "High-assay low enriched uranium" (PDF). energy.gov. Archived (PDF) from the original on 9 October 2022.
  9. ^ "HALEU UF6 and SMR fuel fabrication". Nuclear Engineering International. 30 June 2024. Retrieved 16 July 2024.
  10. ^ Glaser, Alexander (6 November 2005). About the Enrichment Limit for Research Reactor Conversion : Why 20%? (PDF). The 27th International Meeting on Reduced Enrichment for Research and Test Reactors (RERTR. Princeton University. Archived (PDF) from the original on 9 October 2022. Retrieved 18 April 2014.
  11. ^ a b Forsberg, C. W.; Hopper, C. M.; Richter, J. L.; Vantine, H. C. (March 1998). "Definition of Weapons-Usable Uranium-233" (PDF). ORNL/TM-13517. Oak Ridge National Laboratories. Archived from the original (PDF) on 2 November 2013. Retrieved 30 October 2013.
  12. ^ Sublette, Carey (4 October 1996). "Nuclear Weapons FAQ, Section 4.1.7.1: Nuclear Design Principles – Highly Enriched Uranium". Nuclear Weapons FAQ. Retrieved 2 October 2010.
  13. ^ Mosteller, R.D. (1994). "Detailed Reanalysis of a Benchmark Critical Experiment: Water-Reflected Enriched-Uranium Sphere" (PDF). Los Alamos Technical Paper (LA–UR–93–4097): 2. doi:10.2172/10120434. Archived (PDF) from the original on 9 October 2022. Retrieved 19 December 2007. The enrichment of the pin and of one of the hemispheres was 97.67 w/o, while the enrichment of the other hemisphere was 97.68 w/o.
  14. ^ Olander, Donald R. (1 January 1981). "The theory of uranium enrichment by the gas centrifuge". Progress in Nuclear Energy. 8 (1): 1–33. doi:10.1016/0149-1970(81)90026-3. ISSN 0149-1970.
  15. ^ "Nuclear Weapons FAQ". Retrieved 26 January 2013.
  16. ^ Lei, Jia; Liu, Huanhuan; Zhou, Li; Wang, Yazhou; Yu, Kaifu; Zhu, Hui; Wang, Bo; Zang, Mengxuan; Zhou, Jian; He, Rong; Zhu, Wenkun (1 September 2023). "Progress and perspective in enrichment and separation of radionuclide uranium by biomass functional materials". Chemical Engineering Journal. 471: 144586. doi:10.1016/j.cej.2023.144586. ISSN 1385-8947.
  17. ^ Von Hippel, Frank N.; Kahn, Laura H. (December 2006). "Feasibility of Eliminating the Use of Highly Enriched Uranium in the Production of Medical Radioisotopes". Science & Global Security. 14 (2 & 3): 151–162. Bibcode:2006S&GS...14..151V. doi:10.1080/08929880600993071. S2CID 122507063.
  18. ^ "Uranium Enrichment". world-nuclear.org. Archived from the original on 1 July 2013. Retrieved 14 April 2013.
  19. ^ a b c d "Lodge Partners Mid-Cap Conference 11 April 2008" (PDF). Silex Ltd. 11 April 2008. Archived (PDF) from the original on 9 October 2022.
  20. ^ Adams, Rod (24 May 2011). "McConnell asks DOE to keep using 60-year-old enrichment plant to save jobs". Atomic Insights. Archived from the original on 28 January 2013. Retrieved 26 January 2013.
  21. ^ "Paducah enrichment plant to be closed - World Nuclear News". www.world-nuclear-news.org.
  22. ^ a b Lei, Jia; Liu, Huanhuan; Zhou, Li; Wang, Yazhou; Yu, Kaifu; Zhu, Hui; Wang, Bo; Zang, Mengxuan; Zhou, Jian; He, Rong; Zhu, Wenkun (1 September 2023). "Progress and perspective in enrichment and separation of radionuclide uranium by biomass functional materials". Chemical Engineering Journal. 471: 144586. doi:10.1016/j.cej.2023.144586. ISSN 1385-8947.
  23. ^ a b c Weinberger, Sharon (28 September 2012). "US grants licence for uranium laser enrichment". Nature: nature.2012.11502. doi:10.1038/nature.2012.11502. S2CID 100862135.
  24. ^ a b Slakey, Francis; Cohen, Linda R. (March 2010). "Stop laser uranium enrichment". Nature. 464 (7285): 32–33. Bibcode:2010Natur.464...32S. doi:10.1038/464032a. PMID 20203589. S2CID 205053626. ProQuest 204555310.
  25. ^ F. J. Duarte and L. W. Hillman (Eds.), Dye Laser Principles (Academic, New York, 1990) Chapter 9.
  26. ^ "GE Signs Agreement With Silex Systems of Australia To Develop Uranium Enrichment Technology" (Press release). GE Energy. 22 May 2006. Archived from the original on 14 June 2006.
  27. ^ "GE Hitachi Nuclear Energy Selects Wilmington, N.C. as Site for Potential Commercial Uranium Enrichment Facility". Business Wire. 30 April 2008. Retrieved 30 September 2012.
  28. ^ Broad, William J. (20 August 2011). "Laser Advances in Nuclear Fuel Stir Terror Fear". The New York Times. Retrieved 21 August 2011.
  29. ^ Associated Press (27 September 2012). "Uranium Plant Using Laser Technology Wins U.S. Approval". The New York Times.
  30. ^ Becker, E. W.; Ehrfeld, W.; Münchmeyer, D.; Betz, H.; Heuberger, A.; Pongratz, S.; Glashauser, W.; Michel, H. J.; Siemens, R. (1982). "Production of Separation-Nozzle Systems for Uranium Enrichment by a Combination of X-Ray Lithography and Galvanoplastics". Naturwissenschaften. 69 (11): 520–523. Bibcode:1982NW.....69..520B. doi:10.1007/BF00463495. S2CID 44245091.
  31. ^ Smith, Michael; Jackson A G M (2000). "Dr". South African Institution of Chemical Engineers – Conference 2000: 280–289.
  32. ^ Balakrishnan, M. R. (1971). "Economics of blending, a case study" (PDF). Bombay, India: Government of India, Atomic Energy Commission. p. 6. Archived (PDF) from the original on 9 October 2022. Retrieved 7 November 2021.
  33. ^ US Atomic Energy Commission (January 1961). "Costs of nuclear power". Washington DC: Office of Technical Services, Dept of Commerce. p. 29. Retrieved 7 November 2021.
  34. ^ "Status Report: USEC-DOE Megatons to Megawatts Program". USEC.com. 1 May 2000. Archived from the original on 6 April 2001.
  35. ^ "Megatons to Megawatts". centrusenergy.com. December 2013.
  36. ^ Makhijani, Arjun; Chalmers, Lois; Smith, Brice (15 October 2004). Uranium enrichment (PDF). Institute for Energy and Environmental Research. Archived (PDF) from the original on 9 October 2022. Retrieved 21 November 2009.
  37. ^ Australia's uranium - Greenhouse friendly fuel for an energy hungry world (PDF). Standing Committee on Industry and Resources (Report). The Parliament of the Commonwealth of Australia. November 2006. p. 730. Archived (PDF) from the original on 9 October 2022. Retrieved 3 April 2015.
  38. ^ "Q&A: Uranium enrichment". BBC News. BBC. 1 September 2006. Retrieved 3 January 2010.
  39. ^ "Laser enrichment could cut cost of nuclear power". The Sydney Morning Herald. 26 May 2006.
  40. ^ Weinberger, Sharon (28 September 2012). "US grants licence for uranium laser enrichment". Nature. doi:10.1038/nature.2012.11502. ISSN 1476-4687. S2CID 100862135.
  41. ^ "Israel's Nuclear Weapons Program". Nuclear Weapon Archive. 10 December 1997. Retrieved 7 October 2007.
  42. ^ Burr, William (22 December 2015). "Strategic Air Command Declassifies Nuclear Target List from 1950s". nsarchive2.gwu.edu. Retrieved 27 November 2020. Oralloy [Oak Ridge alloy] was a term of art for highly enriched uranium.
[edit]
Look up enriched uranium in Wiktionary, the free dictionary.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Enriched_uranium&oldid=1257121843"