The options for the future production of the medical isotope 99Mo
- 1.7k Downloads
In several countries, the present shortage has given rise to studies on possible ways to resolve the problem. In Canada, it was originally planned to replace the NRU by two so-called MAPLE reactors, but that project was discontinued for technical reasons . Subsequently, at the initiative of the Canadian Government, an independent expert panel reviewed a large number of different proposals for 99Mo production, in order to advise on the way forward . In the USA a committee investigated options to move away from the current use of highly enriched uranium (HEU) as target material for 99Mo production . In the Netherlands, a new multipurpose reactor Pallas  has been proposed. This prompted the Dutch government to commission an independent review of all possibilities to produce 99Mo in the future .
Such an important issue as the production of 99Mo has political, economic and scientific aspects. In this editorial we focus on a scientific comparison of all the options, using the results of the independent committees as a basis. First we discuss the current technology of irradiating HEU plates in reactors. Then we describe the possible alternatives for 99Mo production in four broad categories: molybdenum targets in reactors, target plates in accelerators, 99Mo extraction from liquid reactors and the replacement of the HEU targets by low enriched uranium (LEU). Finally we present conclusions, which are supported by the independent reviews mentioned above.
Current technology: uranium targets in a reactor
Almost all 99Mo production today comes from research reactors. Targets containing uranium are placed inside the reactor, where neutrons cause fission of 235U atoms inside the target. Many isotopes are formed by these fission processes and these include 99Mo, so-called fission product 99Mo. After about 1 week of irradiation, the targets are taken from the reactor for chemical processing. The targets are dissolved in either an acid or alkaline solution and the 99Mo is extracted chemically.
Nuclear reaction types for the various proposals
10-24 cm2 (=barn)
Current, alternative 3, 4
n + 235U → 99Mo + xx + 2n
(586 × 6% =) 35
n + 98Mo → 99Mo
γ + 238U → 99Mo + xx + 2n
0.16 × 6%
γ + 100Mo → 99Mo + n
p + 100Mo → 99Mo + p + n
p + 100Mo → 99mTc + 2n
There are also downsides. The chemical processing of targets creates liquid chemical waste that is highly radioactive and this must be processed and safely stored. Also, the procedure uses HEU, which is strategically sensitive material.
Alternative 1: molybdenum targets in a reactor
A first alternative is to irradiate molybdenum targets in a reactor. Neutrons can be captured by 98Mo atoms to form 99Mo. The chemical processing after irradiation is relatively simple, as one only needs to dissolve the molybdenum target and there is no complicated extraction process. Indeed this process was used for many years before the introduction of fission product 99Mo.
The production rate, however, is a problem. The probability that 98Mo captures a neutron is rather low compared to 235U fission (see Table 1). With the other factors that influence the production rate roughly equal, the production rate from a 98Mo target is 250 times lower than fission, even for an expensive 100% enriched 98Mo target.
Perhaps more importantly, only a tiny fraction of the original molybdenum is converted to 99Mo in the process. The fraction of 99Mo per gram molybdenum is 1,000 times lower compared to the current technology, leading to much lower radioactivity per gram of molybdenum. This low specific activity 99Mo product would not work with today’s 99mTc generators and would cause a problem with some 99mTc imaging kits. The design of the 99mTc generators used to deliver the product to hospitals could be modified. This would have significant impact on the generator and imaging kit technology and it is unclear whether this is feasible to change.
To separate 99Mo from the rest of the molybdenum, there is research  into the possibility of using the recoil of the 99Mo that is caused by the neutron capture of 98Mo. This method requires a target with a very high surface to volume ratio and needs to be scaled up. If this research is fruitful, the problem of the production rate still remains.
GE Hitachi Nuclear Energy (press release, 25 January 2010) will develop a 99Mo production method by placing molybdenum targets in commercial nuclear power reactors. As explained above, this method will have a low production rate. On the other hand, power reactors have the advantage of very large target volumes, so production of large quantities of very low specific activity 99Mo is theoretically possible.
Alternative 2: accelerators
To avoid the use of reactors, accelerators are often proposed. When charged particles such as protons or electrons are accelerated to high enough energies, nuclear reactions can be induced in a target. The most commonly proposed reactions are listed in Table 1. In some cases, high energy photons are proposed instead of charged particles. The method using photon-induced fission of 238U was recently proposed on the basis of computer simulations , but this has yet to be demonstrated and would need to be scaled up for mass production.
Accelerator methods using molybdenum as target material suffer from the same problem as molybdenum targets in reactors: the final product contains mostly inactive molybdenum, because only a tiny fraction of the molybdenum target is converted to 99Mo.
The last reaction shown in Table 1 does not produce 99Mo, but directly produces 99mTc. The 6-h half-life of 99mTc implies that it is only possible to distribute it to a local regional area from a single production centre. Also, another form of technetium (99gTc) is produced simultaneously with the 99mTc in three times larger quantities (A.J. Koning, S. Qaim & M.C. Duijvestijn, to be published). This additional inactive technetium could have negative effects upon some 99mTc imaging kits.
An important advantage of accelerators is that they produce relatively less waste than reactors. Also, most accelerators require less investment than reactors.
The disadvantage of accelerators is the low production rate. For all the reactions listed in Table 1, the interaction probability is more than 250 times lower than the present fission process. In principle the flux of accelerated particles can be made higher than in a reactor, but this requires the development of new, even higher power accelerators. Perhaps more importantly, the useful irradiation volume (target size) in an accelerator is much smaller than in a reactor.
Therefore, the only remedy would be to build many accelerators. Independent expert panels have estimated that 500 accelerators would be needed, of a type that has yet to be developed. This would require a significant research effort and substantial investment with significant risks.
A US Scientific Advisory Committee did recommend, recently, the building of an accelerator for isotope production . This advice, though, was for medical isotopes other than 99Mo, because there is an important category of medical isotopes that can be better produced using accelerators. The worldwide production level required for these isotopes is far lower than for 99Mo.
There are also proposals to couple an accelerator to a sub-critical reactor. The advantage would be that the flux produced by the accelerator is boosted by the chain reaction in the reactor. In essence, however, this option is building both a reactor and an accelerator, instead of just one of them.
Alternative 3: liquid reactors
Instead of placing uranium targets in a reactor or an accelerator, one can also dissolve uranium in water. When one fills a vessel of say 150 l with uranyl nitrate, this can be made critical as an aqueous homogeneous reactor, containing a few kilogram of uranium. Once a week, the solution could be transferred to a hot cell for processing and the molybdenum chemically extracted. Afterwards, the remaining solution has to be fed back into the reactor, otherwise the 99Mo yield per kilogram of uranium would be very low.
The principle of this technology has been proven, with a reactor power of the order of 200 kW. Assuming that all of the 99Mo yield of a liquid reactor could be extracted every week, then, based on a comparison with present experience, around 20 liquid reactors would be required to produce the present world demand.
Advantages of liquid reactors are claimed to be an efficient use of neutrons, elimination of targets and lower costs.
The drawback of this technology is that it is not yet mature. An International Atomic Energy Agency (IAEA) report  lists many items that need further research, starting with determining whether this reactor type can be operated reliably for prolonged periods. The combination of the uranium solution and chemical processing has to be optimized, especially in view of the need to recycle the solution. This also means that the chemical cocktail in the reactor will be different after every production run. Since this reactor type is new, the license process for building and operating the reactor will be in uncharted territory. The suitability of the final 99Mo product in existing 99mTc generator designs is also not known.
The companies Babcock & Wilcox (press release, 26 January 2009) and Covidien have announced a project to develop this technology.
Alternative 4: conversion from HEU to LEU
There is the possibility to continue operations with more or less the current technology, but replacing HEU targets by LEU ones. LEU has by definition less than 20% of the fissile isotope 235U. The present targets for 99Mo production, though, are so far still made of HEU, for the reasons outlined below.
When an HEU target is directly replaced by an equivalent LEU target, the number of 235U atoms is reduced by a factor of 5, and so is the 99Mo production rate. To counter this effect, a different alloy of uranium and aluminium with increased uranium density can be used and thicker targets made. Such targets are currently used in Argentina for 99Mo production to serve the local market. Compared to the current technology, these targets have a two to three times lower 99Mo yield.
Materials are under development with even higher uranium densities. An example is the uranium silicide that is used as reactor fuel in the HFR, but it is not easy to chemically extract the molybdenum from this material. There are also alloys of uranium and molybdenum with very high uranium densities, but these alloys encounter the same problem as molybdenum targets: the initial molybdenum in the target also ends up in the final product leading to low specific activity 99Mo.
The use of molybdenum targets leads to an activity per gram of molybdenum that is low. Even if this problem could be solved, the production quantities will be low.
Accelerators have a low production rate, so many of them would be needed to cover world supply. Direct production of 99mTc has a lower activity per gram of technetium giving potential technical problems and has a logistic limitation because of the 99mTc half-life of 6 h.
Liquid reactors hold a promise for the future, but parts of the necessary technology need further research. The license process and the operational challenges and economics of this type of reactor are presently unknown. A significant number of liquid reactors would be needed to cover world supply.
Conversion of the HEU targets to LEU, using currently available technology, leads to a reduction in production capacity by a factor of 2–3. Given the current crisis in production levels, it is difficult to see how this conversion can be implemented in the short term and without building additional reactor capacity.
Reactors will therefore remain necessary for the foreseeable future. The best way to secure the supply of 99Mo for the more than 30 million patients each year is to build new research reactors to replace the old ones and to ensure sufficient total production capacity worldwide.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
- 1.Verbeek P. Report on molybdenum-99 production for nuclear medicine 2010–2020. AIPES Report, November 2008.Google Scholar
- 2.Technopolis Group. Radioisotopes in medicine. Foresight of the use of reactor isotopes until 2025. Technopolis Report, December 2008.Google Scholar
- 3.Labrie JP. Look beyond MAPLE reactors for isotope shortage answer. Canadian National Post, 28 July 2008.Google Scholar
- 4.Goodhand P, Drouin R, Mason T, Turcotte E. Report of the Expert Review Panel on Medical Isotope Production. Canada, 30 November 2009.Google Scholar
- 5.Whipple C, et al. Medical isotope production without highly enriched uranium. National Academy of Sciences Report, ISBN 0-309-13040-9; 2009.Google Scholar
- 6.Pallas reactor. www.pallasreactor.eu/home/news. 2009.
- 7.Bode P, Delorme T. Productiewijzen voor radionucliden voor medische toepassingen met een onderzoeks-kernreactor en alternatieve technologieën. TU Delft report TUD-RID 2009-001, 11 February 2009.Google Scholar
- 8.Tomar BS, Steinebach OM, Bode P, Wolterbeek HT. Increasing the specific activity of medically useful isotopes through Szilard Chalmers reaction. Trans Am Nucl Soc 2008:880–1.Google Scholar
- 11.Homogenous aqueous solution nuclear reactors for the production of Mo-99 and other short lived radioisotopes. IAEA-TECDOC-1601, September 2008.Google Scholar