Synthesis of precious metals
The synthesis of precious metals, a symbolic goal long sought by alchemists, is only possible with methods utilizing nuclear physics, currently involving either nuclear reactors or particle accelerators. Since particle accelerators require huge amounts of energy while nuclear reactors produce energy, production methods using a nuclear reactor are considered more economically feasible. Often the goal of synthesis is to produce an element at a cost significantly less than the standard methods of production. Recovery of rare elements from spent fuel rods is also anticipated to help offset the cost of reprocessing.
- 1 Precious metals occurring as fission products
- 2 Precious metals produced via irradiation
- 3 See also
- 4 References
- 5 External links
Precious metals occurring as fission products
Ruthenium and rhodium are precious metals produced by nuclear fission, as a small percentage of the fission products. The radioisotopes of these elements generated by nuclear fission with the longest half-lives have half-lives of 373.59 days and 45 days for ruthenium and rhodium, respectively. This makes their extraction from spent nuclear fuel possible, although they must be checked for radioactivity before use.
Until now no facility has been reprocessing spent nuclear fuels for ruthenium and rhodium; however, Japan is planning to do so in their new spent fuel reprocessing facility, which will help offset the cost of reprocessing.
Each kilogram of the fission products of 235U will contain 63.44 grams of ruthenium isotopes with halflives longer than a day. Since a typical used nuclear fuel contains about 3% fission products, one ton of used fuel will contain about 1.9 kg of ruthenium. The 103Ru and 106Ru will render the fission ruthenium very radioactive. If the fission occurs in an instant then the ruthenium thus formed will have an activity due to 103Ru of 109 TBq g−1 and 106Ru of 1.52 TBq g−1. 103Ru has a half-life of about 39 days meaning that within 390 days it will have effectively decayed to the only stable isotope of rhodium, 103Rh, well before any reprocessing is likely to occur. 106Ru has a half-life of about 373 days, meaning that if the fuel is left to cool for 5 years before reprocessing only about 3% of the original quantity will remain; the rest will have decayed.
It is also possible to extract rhodium from used nuclear fuel, which contains rhodium—1 kg of the fission products of 235U contains 13.3 grams of 103Rh. Therefore, as typical used fuel is 3% fission products by weight, it will contain about 400 grams of rhodium per ton of used fuel. The longest lived radioisotope of rhodium is 102mRh, which has a half-life of 2.9 years, while the ground state (102Rh) has a half-life of 207 days.
Each kilogram of fission rhodium will contain 6.62 ng of 102Rh and 3.68 ng of 102mRh. As 102Rh decays by beta decay to either 102Ru (80%) (some Positron emission will occur) or 102Pd (20%) (some gamma ray photons with about 500 keV are generated) and the excited state decays by beta decay (electron capture) to 102Ru (some gamma ray photons with about 1 MeV are generated). If the fission occurs in an instant then 13.3 grams of rhodium will contain 67.1 MBq (1.81 mCi) of 102Rh and 10.8 MBq (291 μCi) of 102mRh. As it is normal to allow used nuclear fuel to stand for about five years before reprocessing, much of this activity will decay away leaving 4.7 MBq of 102Rh and 5.0 MBq of 102mRh. If the rhodium metal was then left for 20 years after fission then the 13.3 grams of rhodium metal would contain 1.3 kBq of 102Rh and 500 kBq of 102mRh. At first glance the rhodium might be adding to the resource value of reprocessed fission waste, as rhodium has the highest price of any precious metal ($97,000/kg in early 2010), but the cost of the separation of the rhodium from the other metals needs to be considered.
Palladium is also produced by nuclear fission in small percentages, amounting to 1 kg per ton of spent fuel. As opposed to rhodium and ruthenium, palladium has a radioactive isotope, 107Pd, with a very long half-life (6.5 million years), so palladium produced in this way has a very low radioactive intensity. Mixed in with the other isotopes of palladium recovered from the spent fuel, this gives a radioactive dose rate of 7.207x10−5 Ci, which is well below the safe level of 1x10−3 Ci. Also, 107Pd has a very low decay energy of only 33 KeV, and so would be unlikely to pose a hazard even if pure.
Silver is produced as result of nuclear fission in small amounts (approximately 0.1%). Because of this, extraction of silver from highly radioactive fission products would be uneconomical, but when recovered with palladium, rhodium and ruthenium (price of silver in 2011: about 880 €/kg; rhodium; and ruthenium: about 300,000 €/kg) the economics change substantially. Silver becomes a byproduct of platinoid metal recovery from fission waste.
Precious metals produced via irradiation
In addition to being a fission product of uranium, as described above, another way to produce ruthenium is to start with molybdenum, which has a price averaging between $10 and $20/kg, in contrast with ruthenium's $5500/kg. The isotope 100Mo, which has an abundance of 9.6% in natural molybdenum, can be transmuted to 101Mo by slow neutron irradiation. 101Mo and its daughter product, 101Tc, both have beta-decay half-lives of roughly 14 minutes. The end product is stable 101Ru.
In addition to being a fission product of uranium, as described above, another way to produce rhodium is to start with ruthenium, which has a price of $5500/kg, which is much lower than rhodium's $97,000/kg. The isotope 102Ru, which forms 31.6% of natural ruthenium, can be transmuted to 103Ru by slow neutron irradiation. 103Ru then decays to 103Rh via beta decay, with a half-life of 39.26 days. The isotopes 98Ru through 101Ru, which together form 44.2% of natural ruthenium, could also be transmuted into 102Ru, and subsequently to 103Ru and then 103Rh, through multiple neutron captures in a nuclear reactor.
The cost of rhenium as of January 2010 was $6,250/kg; by contrast, tungsten is very cheap, with a price of under $30/kg as of July 2010. The isotopes 184W and 186W together make up roughly 59% of naturally-occurring tungsten. Slow-neutron irradiation could convert these isotopes into 185W and 187W, which have half-lives of 75 days and 24 hours, respectively, and always undergo beta decay to the corresponding rhenium isotopes. These isotopes could then be further irradiated to transmute them into osmium (see below), increasing their value further. Also, 182W and 183W, which together form 40.8% of naturally-occurring tungsten, can, via multiple neutron captures in a nuclear reactor, be transmuted into 184W, which can then be transmuted into rhenium.
The cost of osmium as of January 2010 was $12,217 per kilogram, making it roughly twice the price of rhenium, which is worth $6,250/kg. Rhenium has two naturally occurring isotopes, 185Re and 187Re. Irradiation by slow neutrons would transmute these isotopes into 186Re and 188Re, which have half-lives of 3 days and 17 hours, respectively. The predominant decay pathway for both of these isotopes is beta-minus decay into 186Os and 188Os.
The cost of iridium as of January 2010 was $13,117/kg, somewhat higher than that of osmium ($12,217/kg). The isotopes 190Os and 192Os together make up roughly 67% of naturally-occurring osmium. Slow-neutron irradiation could convert these isotopes into 191Os and 193Os, which have half-lives of 15.4 and 30.11 days, respectively, and always undergo beta decay to 191Ir and 193Ir, respectively. Also, 186Os through 189Os could be transmuted into 190Os through multiple neutron captures in a nuclear reactor, and subsequently into iridium. These isotopes could then be further irradiated to transmute them into platinum (see below), increasing their value further.
The cost of platinum as of January 2010 was $49,995 per kilogram, making it the second most expensive precious metal after rhodium. Iridium, by contrast, has only about one-fourth the value of platinum ($13,117/kg). Iridium has two naturally occurring isotopes, 191Ir and 193Ir. Irradiation by slow neutrons would transmute these isotopes into 192Ir and 194Ir, with short half-lives of 73 days and 19 hours, respectively; the predominant decay pathway for both of these isotopes is beta-minus decay into 192Pt and 194Pt.
Chrysopoeia, the artificial production of gold, is the symbolic goal of alchemists. Alchemists often understood this as a metaphor for a mystical, philosophical, psychological, medical, or religious transformation. Despite this, some alchemists interpreted this literally, and attempted to physically transmute base metals into gold. Such transmutation is possible in particle accelerators or nuclear reactors, although the production cost is currently many times the market price of gold. Since there is only one stable gold isotope, 197Au, nuclear reactions must create this isotope in order to produce usable gold.
Gold synthesis in an accelerator
Gold synthesis in a particle accelerator is possible in many ways. The Spallation Neutron Source has a liquid mercury target which will be transmuted into gold, platinum, and iridium, which are lower in atomic number than mercury.
Gold synthesis in a nuclear reactor
Gold was synthesized from mercury by neutron bombardment in 1941, but the isotopes of gold produced were all radioactive. In 1924, a Japanese physicist, Hantaro Nagaoka, accomplished the same feat.
Only the mercury isotope 196Hg, which occurs with a frequency of 0.15% in natural mercury, can be converted to gold by slow neutron capture, and following electron capture, decay into gold's only stable isotope, 197Au. When other mercury isotopes are irradiated with slow neutrons, they also undergo neutron capture, but either convert into each other or beta decay into the thallium isotopes 203Tl and 205Tl.
Using fast neutrons, the mercury isotope 198Hg, which composes 9.97% of natural mercury, can be converted by splitting off a neutron and becoming 197Hg, which then disintegrates to stable gold. This reaction, however, possesses a smaller activation cross-section and is feasible only with un-moderated reactors.
It is also possible to eject several neutrons with very high energy into the other mercury isotopes in order to form 197Hg. However such high-energy neutrons can be produced only by particle accelerators.[clarification needed].
In 1980, Glenn Seaborg transmuted several thousand atoms of bismuth into gold at the Lawrence Berkeley Laboratory. His experimental technique, using nuclear physics, was able to remove protons and neutrons from the bismuth atoms. Seaborg's technique would have been far too expensive to enable the routine manufacture of gold, however.
- Bush, R. P. (1991). "Recovery of Platinum Group Metals from High Level Radioactive Waste". Platinum Metals Review 35 (4): 202–208.
- "Molybdenum Price". Retrieved July 25, 2010.
- "Tungsten Prices".
- "Iridium 194".
- "Iridium 192".
- R. Sherr, K. T. Bainbridge, and H. H. Anderson (1941). "Transmutation of Mercury by Fast Neutrons". Physical Review 60 (7): 473–479. Bibcode:1941PhRv...60..473S. doi:10.1103/PhysRev.60.473.
- A.Miethe, ”Der Zerfall des Quecksilberatoms,” Naturwissenschaften, 12(1924): 597-598
- Aleklett, K.; Morrissey, D.; Loveland, W.; McGaughey, P.; Seaborg, G. (1981). "Energy dependence of 209Bi fragmentation in relativistic nuclear collisions". Physical Review C 23 (3): 1044. Bibcode:1981PhRvC..23.1044A. doi:10.1103/PhysRevC.23.1044.
- Matthews, Robert (2 December 2, 2001). "The Philosopher's Stone". The Daily Telegraph. Retrieved July 23, 2013. Check date values in:
- Spallation Neutron Source
- Mercury 197
- Mercury 197 decays to Gold 197
- Kolarik, Zdenek; Renard, Edouard V. (2005). "Potential Applications of Fission Platinoids in Industry". Platinum Metals Review 49 (2): 79. doi:10.1595/147106705X35263.
- Kolarik, Zdenek; Renard, Edouard V. (2003). "Recovery of Value Fission Platinoids from Spent Nuclear Fuel. Part I PART I: General Considerations and Basic Chemistry". Platinum Metals Review 47 (2): 74–87.
- Kolarik, Zdenek; Renard, Edouard V. (2003). "Recovery of Value Fission Platinoids from Spent Nuclear Fuel. Part II: Separation Process". Platinum Metals Review 47 (2): 123–131.