Molten Salt Reactors
(Updated 8 September 2016)
- Molten salt reactors operated in the 1960s.
- They are seen as a promising technology today principally as a thorium fuel cycle prospect or for using spent LWR fuel.
- A variety of designs is being developed, some as fast neutron types.
- Global research is currently led by China.
- Some have solid fuel similar to HTR fuel.
- Others have fuel dissolved in the molten salt coolant.
Molten salt reactors (MSRs) use molten fluoride salts as primary coolant, at low pressure. This itself is not a radical departure when the fuel is solid and fixed. But extending the concept to dissolving the fissile and fertile fuel in the salt certainly represents a leap in lateral thinking relative to nearly every reactor operated so far. However, the concept is not new, as outlined below.
MSRs may operate with epithermal or fast neutron spectrums, and with a variety of fuels. Much of the interest today in reviving the MSR concept relates to using thorium (to breed fissile uranium-233). There are a number of different MSR design concepts, and a number of interesting challenges in the commercialisation of many, especially with thorium.
The salts concerned as primary coolant, mostly lithium-beryllium fluoride and lithium fluoride, remain liquid without pressurization from about 500°C up to about 1400°C, in marked contrast to a PWR which operates at about 315°C under 150 atmospheres pressure.
The main MSR concept is to have the fuel dissolved in the coolant as fuel salt, and ultimately to reprocess that online. Batch reprocessing is likely in the short term, and fuel life is quoted at 4-7 years, with high burn-up. Intermediate designs and the AHTR have fuel particles in solid graphite and have less potential for thorium use.
During the 1960s, the USA developed the molten salt breeder reactor concept at the Oak Ridge National Laboratory, Tennessee (built as part of the wartime Manhattan Project). It was the primary back-up option for the fast breeder reactor (cooled by liquid metal) and a small prototype 8 MWt Molten Salt Reactor Experiment (MSRE) operated at Oak Ridge over four years to 1969 (the MSR programme ran 1957-1976). In the first campaign (1965-68), uranium-235 tetrafluoride (UF4) enriched to 33% was dissolved in molten lithium, beryllium and zirconium fluorides at 600-700°C which flowed through a graphite moderator at ambient pressure. The fuel comprised about one percent of the fluid.
The coolant salt in a secondary circuit was lithium + beryllium fluoride (FLiBe).* There was no breeding blanket, this being omitted for simplicity in favour of neutron measurements.
The original objectives of the MSRE were achieved by March 1965, and the U-235 campaign concluded. A second campaign (1968-69) used U-233 fuel which was then available, making MSRE the first reactor to use U-233, though it was imported and not bred in the reactor. This program prepared the way for building a MSR breeder utilising thorium, which would operate in the thermal (slow) neutron spectrum.
According to NRC 2007, the culmination of the Oak Ridge research over 1970-76 resulted in a MSR design that would use LiF-BeF2-ThF4-UF4 (72-16-12-0.4) as fuel. It would be moderated by graphite with a four-year replacement schedule, use NaF-NaBF4 as the secondary coolant, and have a peak operating temperature of 705°C.
The R&D program demonstrated the feasibility of this system, albeit excluding online reprocessing, and highlighted some unique corrosion and safety issues that would need to be addressed if constructing a larger pilot MSR with fuel salt. Challenges would include processing facilities to remove the main fission products, though gaseous fission products come off readily in the gas purge system. It also showed that breeding required a different design, with a larger blanket loop and two fluids (heterogeneous). Tritium production was a problem (see below re lithium enrichment).
In 1980 Oak Ridge published a study to "examine the conceptual feasibility” of a denatured MSR (DMSR) fuelled with low-enriched uranium-235 “and operated with a minimum of chemical processing," solely as a burner reactor. The main priority was proliferation resistance, avoiding use of HEU.
In the UK a large (2.5 GWe) lead-cooled fast spectrum MSR (MSFR) with the plutonium fuel dissolved in a molten chloride salt was designed, with experimental work undertaken over 1968-73. Funding ceased in 1974.
There is now renewed interest in the MSR concept in Japan, Russia, China, France and the USA, and one of the six Generation IV designs selected for further development is the MSR in two distinct variants, the molten salt fast reactor (MSFR) and the advanced high temperature reactor (AHTR) – also known as the fluoride salt-cooled high-temperature reactor (FHR) with solid fuel, or PB-FHR specifically with pebble fuel. The Generation IV international Forum (GIF) mentions 'salt processing' as a technology gap for MSRs, putting the initial focus clearly on burners rather than breeders.
Since the 2002 Generation IV selection process, significant changes in design philosophy have taken place, according to a 2015 report by Energy Process Developments Ltd (EPD). The first is to design simpler, less ambitious, molten salt reactors that do not breed new fuel, do not require online fuel reprocessing and which use the well-established enriched uranium fuel cycle. In this regard, both American researchers and the China Academy of Sciences/SINAP are working on solid fuel, salt-cooled reactor technology as a realistic first step into MSRs. In 2014, as part of an assessment of MSR activity internationally, proposals were made for pilot-scale implementation, where technical readiness was claimed. Six such specific proposals* were assessed over 12 months with commissioned expertise from established UK nuclear engineering firms. These proposals were all seen as credible for building a prototype, with one emerging in the EPD report as currently most suitable as a basis for UK MSR development, the Moltex SSR.
* from Flibe Energy, ThorCon, Moltex, Seaborg Technologies, Terrestrial Energy and Transatomic Power.
In the normal or basic MSR concept, the fuel is a molten mixture of lithium and beryllium fluoride (FLiBe) salts with dissolved low-enriched uranium (U-235 or U-233) fluorides (UF4). The core consists of unclad graphite moderator arranged to allow the flow of salt at about 700°C and at low pressure. Much higher temperatures are possible but not yet tested. Heat is transferred to a secondary salt circuit and thence to steam or process heat. The basic design is not a fast neutron reactor, but with some moderation by the graphite is epithermal (intermediate neutron speed) and breeding ratio is less than 1.
However, this concept, with fuel dissolved in the salt, is further from commercialisation than solid fuel designs, where the ceramic fuel may be set in prisms, plates, or pebbles, or one design with liquid fuel in static tubes. Reprocessing that fuel salt online is even further from commercialization.
Considering liquid-fuel MSR designs, thorium can be dissolved with the uranium in a single fluid MSR, known as a homogeneous design. Two-fluid, or heterogeneous MSRs, would have fertile salt containing thorium in a second loop separate from the fuel salt containing fissile uranium or plutonium and could operate as a breeder reactor (MSBR). Here, the U-233 is progressively removed* and transferred to the primary circuit. However, graphite degradation from neutron flux limits the useful life of the reactor core with the fuel and breeding fluids in close juxtaposition, and in the 1960s it was assumed that the entire reactor vessel in the two-fluid design would be replaced after about eight years.**
In liquid-fuel MSR designs the fission products dissolve in the fuel salt and are ideally removed continuously in an adjacent online reprocessing loop and replaced with fissile uranium, plutonium and other actinides or, potentially, fertile Th-232 or U-238. Meanwhile caesium and iodine in particular remain secure in the molten salt. Xenon is removed rapidly by outgassing, but protactinium-233 is a problem with thorium as a fuel source. (It is an intermediate product in producing U-233 and is a major neutron absorber.) Constant removal of fission products means that a much higher fuel burn-up could be achieved (> 50%) and the removal of fission products means less decay heat to contend with after reactor shutdown. Actinides are fully recycled and remain in the reactor until they fission or are converted to higher actinides which do so. Hence fissile plutonium is largely consumed, and contributes significant energy. The high-level waste would comprise fission products only, hence with shorter-lived radioactivity.
Compared with solid-fuelled reactors, MSR systems with circulating fuel salt are claimed to have lower fissile inventories*, no radiation damage constraint on fuel burn-up, no requirement to fabricate and handle solid fuel or solid used fuel, and a homogeneous isotopic composition of fuel in the reactor. Actinides are less-readily formed from U-233 than in fuel with atomic mass greater than 235. These and other characteristics may enable MSRs to have unique capabilities and competitive economics for actinide burning and extending fuel resources. Safety is high due to passive cooling up to any size. Also, several designs have freeze plugs so that if excessive temperatures are reached, the primary salt will be drained by gravity away from the moderator into dump tanks configured to prevent criticality.
MSRs have large negative temperature and void coefficients of reactivity, and are designed to shut down due to expansion of the fuel salt as temperature increases beyond design limits. The negative temperature and void reactivity coefficients passively reduce the rate of power increase in the case of an inadvertent control rod withdrawal (technically known as a ‘reactivity insertion’). When tests were made on the MSRE, a control rod was intentionally withdrawn during normal reactor operations at full power (8 MWt) to observe the dynamic response of core power. Such was the rate of fuel salt thermal expansion that reactor power levelled off at 9 MWt without any operator intervention.
The MSR thus has a significant load-following capability where reduced heat abstraction through the boiler tubes leads to increased coolant temperature, or greater heat removal reduces coolant temperature and increases reactivity. Primary reactivity control is using the secondary coolant salt pump or circulation which changes the temperature of the fuel salt in the core, thus altering reactivity due to its strong negative reactivity coefficient. The MSR works at near atmospheric pressure, eliminating the risk of explosive release of volatile radioactive materials.
In the MSBR, the reactor-grade U-233 bred in the secondary circuit needs to be removed, or it will fission there and contaminate that circuit with ‘hot’ fission products. Therefore in practice the protactinium (Pa-233) formed from the thorium needs to be removed before it decays to U-233*, but this process is unproven at any scale. It is relatively easy to remove the U-233 from the Pa-233 by fluorination to UF6 before reducing it to UF4 for adding to the primary fuel salt circuit. However, the U-233 is contaminated with up to 400 ppm U-232 which complicates processing, due to its highly gamma-active decay progeny.
MSRs would normally operate at much higher temperatures than LWRs – up to at least 700°C, and hence have potential for process heat. Up to this temperature, satisfactory structural materials are available. ‘Alloy N’ is a nickel-based alloy (Ni-Cr-Mo-Si) developed at ORNL specifically for MSRs with fluoride salts.
Primary and secondary cooling, the fluoride salts
Fluoride salts have very low vapour pressure even at red heat, carry more heat than the same volume of water, have reasonably good heat transfer properties, are not damaged by radiation, do not react violently with air or water, and are inert to some common structural metals. However having the fuel in solution also means that the primary coolant salt becomes radioactive, complicating maintenance procedures, and the chemistry of the salt must be monitored closely to maintain a chemically reduced state to minimise corrosion. Also the beryllium in the salt is toxic, which leads to at least one design avoiding it, though this requires higher temperatures to keep LiF liquid. LiF however can carry a higher concentration of uranium than FLiBe, allowing less enrichment. There are difficulties with plutonium and other TRU fluorides in fluoride solvents.
Lithium used in the salt must be fairly pure Li-7, since Li-6 produces tritium when fissioned by neutrons. Li-7 has a very small neutron cross-section (0.045 barns). This means that lithium must be enriched beyond its natural 92.5% Li-7 level. Lithium-7 is being produced at least in Russia and possibly China today as a by-product of enriching lithium-6 to produce tritium for thermonuclear weapons. See also Lithium paper.
LiF is exceptionally stable chemically, and the LiF-BeF2 mix ('FLiBe')* is eutectic (at 459°C it has a lower melting point than either ingredient – LiF is about 500°C). It boils at 1430°C. It is favoured in MSR and AHTR primary cooling and when uncontaminated has a low corrosion effect. The three nuclides (Li-7, Be, F) are among the few to have low enough thermal neutron capture cross-sections not to interfere with fission reactions.
LiF without the toxic beryllium solidifies at about 500°C and boils at about 1200°C. FLiNaK (LiF-NaF-KF) is also eutectic and solidifies at 454°C and boils at 1570°C. It has a higher neutron cross-section than FLiBe or LiF but can be used in intermediate cooling loops. Sodium-beryllium fluoride (BeF2-NaF) solidifying at 385°C is used as fuel salt in one design for cost reasons.
The hot molten salt in the primary circuit can be used with secondary salt circuit or secondary helium coolant generating power via the Brayton cycle as with HTR designs, with potential thermal efficiencies of 48% at 750°C to 59% at 1000°C, or simply with steam generators. In industrial applications molten fluoride salts (possibly simply cryolite – Na-Al fluoride) are a preferred interface fluid in a secondary circuit between the nuclear heat source and any chemical plant. The aluminium smelting industry provides substantial experience in managing them safely.
Most secondary coolant salts do not use lithium, for cost reasons. ZrF4-NaF-KF, ZrF4-KF, NaF-BeF2 eutectic mixes are usual, as well as LiF-NaF-KF (FLiNaK).
In the secondary cooling circuit of the AHTR concept, air is compressed, heated, flows through gas turbines producing electricity, enters a steam recovery boiler producing steam that produces additional electricity, and exits to the atmosphere. Added peak power can be produced by injecting natural gas (or hydrogen in the future) after nuclear heating of the compressed air to raise gas temperatures and plant output, giving it rapidly variable output (of great value in grid stability and for peak load demand where renewables have significant input). This is described as an air Brayton combined-cycle (ABCC) system in secondary circuit.
In the 1960s MSRE, an alternative secondary coolant salt considered was 8% NaF + 92% NaF-BeF2 with melting point 385°C, though this would be more corrosive.
Chloride salts, fast-spectrum reactors
Chloride salts have some attractive features compared with fluorides, in particular the actinide trichlorides form lower melting point solutions and have higher solubility for actinides so can contain significant amounts of transuranic elements. PuCl3 in NaCl has been well researched. While NaCl has good nuclear, chemical and physical properties its high melting point means it needs to be blended with MgCl2 or CaCl2, the former being preferred in eutectic, and allowing the addition of actinide trichlorides. The major isotope of chlorine, Cl-35 gives rise to Cl-36 as an activation product – a long-lived energetic beta source, so Cl-37 is much preferable in a reactor.
A British design contains the chloride fuel salt in vertical tubes and relies on convection to circulate the secondary salt coolant, which is a fluoride mix.
Fast spectrum MSRs can have conversion ratios ranging from burner to converter to breeder. This may be within a single unit as the ratio of U-238 to transuranics (TRU) is varied – less U-238 giving more fission. They can be optimised for burning minor actinides, for breeding plutonium from U-238, or they may be open-cycle power plants without heavy metal separation from fission products. The fast neutron spectrum allows the possibility of not having on-site processing to remove TRUs. While fission products have relatively large neutron capture cross sections in the thermal energy range, the capture cross sections at higher energies is much lower, allowing much greater fission product build-up in an MSFR than in a thermal-spectrum MSR (gaseous fission products separate out of the liquid fuel). Eventually the fuel salt heavily loaded with fission products can be sent occasionally for batch processing or allowed to solidify and be disposed of in a repository. For full breeder configuration the fissile material needs to be progressively removed.
MSFRs have a negative void coefficient in the salt and a negative thermal reactivity feedback, so can maintain a high power density with passive safety. Freeze plugs to drain the fuel salt are a further passive safety measure as in other MSRs.
MSR research emphasis
American researchers and the China Academy of Sciences/ SINAP are working primarily on solid fuel MSR technology. The main reason is that this is a realistic first step. In China this is focused on thorium-fueled versions (see LFTR/ TMSR below). The technical difficulty of using molten salts is significantly lower when they do not have the very high activity levels associated with them bearing the dissolved fuels and wastes. The experience gained with component design, operation, and maintenance with clean salts makes it much easier then to move on and consider the use of liquid fuels, while gaining several key advantages from the ability to operate reactors at low pressure and deliver higher temperatures.
Russia's Molten Salt Actinide Recycler and Transmuter (MOSART) is a fast reactor fuelled only by transuranic (TRU) fluorides from uranium and MOX LWR used fuel. It is part of the MARS project (minor actinide recycling in molten salt) involving RIAR, Kurchatov and other research organisations. The 2400 MWt design has a homogeneous core of Li-Na-Be or Li-Be fluorides without graphite moderator and has reduced reprocessing compared with original US design. Thorium may also be used, though it is described as a burner-converter rather than a breeder.
In the Generation IV program for the MSR, collaborative R&D is pursued by interested members under the auspices of a provisional steering committee. There will be a long lead time to prototypes, and the R&D orientation has changed since the project was set up, due to increased interest. It now has two baseline concepts:
- The Molten Salt Fast Neutron Reactor (MSFR), which will take in thorium fuel cycle, recycling of actinides, closed Th/U fuel cycle with no U enrichment, with enhanced safety and minimal wastes. it is a liquid-fuel design.
- The Advanced High-Temperature Reactor (AHTR) – also known as the fluoride salt-cooled high-temperature reactor (FHR) – with the same graphite and solid fuel core structures as the VHTR and molten salt as coolant instead of helium, enabling power densities 4 to 6 times greater than HTRs and power levels up to 4000 MWt with passive safety systems. A 5 MWt prototype is under construction at Shanghai Institute of Nuclear Applied Physics (SINAP, under the China Academy of Sciences) with 2015 target for operation.
The GIF 2014 Roadmap said that a lot of work needed to be done on salts before demonstration reactors were operational, and suggested 2025 as the end of the viability R&D phase.
The SAMOFAR (Safety Assessment of the Molten Salt Fast Reactor) project, based in the Netherlands and funded by the European Commission, aims to prove the safety concepts of the MSFR in breeding mode from thorium. It plans advanced experimental and numerical techniques, to deliver a breakthrough in nuclear safety and optimal waste management, and to create a consortium of stakeholders. "The use of the Th-U fuel cycle is of particular interest to the MSR, because this reactor is the only one in which the Pa-233 can be stored in a hold-up tank to let it decay to U-233." The SAMOFAR consortium consists of 11 participants and is mainly undertaken by universities and research laboratories such as CNRS, JRC, CIRTEN, TU Delft and PSI, thereby exploiting each other’s expertise and infrastructure. It commenced in 2015.
China's dual programme
The China Academy of Sciences in January 2011 launched an R&D program on LFTR, known there as the thorium-breeding molten-salt reactor (Th-MSR or TMSR), and claimed to have the world's largest national effort on it, hoping to obtain full intellectual property rights on the technology. The TMSR Research Centre has a 5 MWe MSR prototype under construction at Shanghai Institute of Applied Physics (SINAP, under the Academy) originally with 2015 target for operation, now 2020.
SINAP has two streams of TMSR development – solid fuel (TRISO in pebbles or prisms/blocks) with once-through fuel cycle, and liquid fuel (dissolved in FLiBe coolant) with reprocessing and recycle. A third stream of fast reactors to consume actinides from LWRs is planned.
- The TMSR-SF stream has only partial utilization of thorium, relying on some breeding as with U-238, and needing fissile uranium input as well. SINAP aims at a 2 MW pilot plant (TMSR-SF1) initially, and a 100 MWt experimental pebble bed plant (TMSR-SF2) with open fuel cycle by about 2025, then a 1 GW demonstration plant (TMSR-SF3) by 2030. TRISO particles will be with both low-enriched uranium and thorium, separately.
- The TMSR-LF stream claims full closed Th-U fuel cycle with breeding of U-233 and much better sustainability with thorium but greater technical difficulty. SINAP aims for a 2 MWt pilot plant (TMSR-LF1) by 2018, a 10 MWt experimental reactor (TMSR-LF2) by 2025 and a 100 MWt demonstration plant (TMSR-LF3) with full electrometallurgical reprocessing by 2035, followed by 1 a GW demonstration plant.
- A TMSFR-LF fast reactor optimized for burning minor actinides is to follow.
SINAP sees molten salt fuel being superior to the TRISO fuel in effectively unlimited burn-up, less waste, and lower fabricating cost, but achieving lower temperatures (600°C+) than the TRISO fuel reactors (1200°C+). Near-term goals include preparing nuclear-grade ThF4 and ThO2 and testing them in a MSR.
The US Department of Energy is collaborating with the China Academy of Sciences on the program, which had a start-up budget of $350 million. The target date for TMSR commercial deployment is 2032.
Other solid- or fixed-fuel types
AHTR / FHR
Research on molten salt coolant has been revived at Oak Ridge National Laboratory (ORNL) in the USA with the Advanced High Temperature Reactor (AHTR). This is a larger reactor using a coated-particle graphite-matrix fuel like that in the GT-MHR (see Small Reactors paper) and with molten fluoride salt as primary coolant. It is also known as the Fluoride High-temperature Reactor (FHR). While similar to the gas-cooled HTR it operates at low pressure (less than 1 atmosphere) and higher temperature, and gives better heat transfer than helium. The FLiBe salt is used solely as coolant, and achieves temperatures of 750-1000°C or more while at low pressure. This could be used in thermochemical hydrogen manufacture.
This could be used in thermochemical hydrogen manufacture. As noted above, a 5 MW thorium-fueled prototype is under construction at Shanghai Institute of Nuclear Applied Physics (SINAP, under the China Academy of Sciences) originally with 2015 target for operation. A 100 MWt demonstration pebble bed plant with open fuel cycle is planned by about 2025. SINAP sees this design having potential for higher temperatures than MSRs with fuel salt.
A small version of AHTR/FHR is the SmAHTR, with 125 MWt thermal size matched to early process heat markets, or producing 50+MWe. Operating temperature is 700°C with FLiBe primary coolant and three integral heat exchangers. It is truck transportable, being 9m long and 3.5m diameter. Fuel is 19.75% enriched uranium in TRISO particles in graphite blocks or fuel plates. Refuelling interval is 2.5 to 4 years depending on fuel configuration. Secondary coolant is FLiNaK to Brayton cycle, and for passive decay heat removal, separate auxiliary loops go to air-cooled radiators. Later versions are intended to reach 850° to 1000°C, using materials yet to be developed.
In the USA a consortium including UC Berkeley, ORNL and Westinghouse is designing a 100 MWe pebble bed FHR, with annular core. It is designed for modular construction, and from 100 MWe base-load is able to deliver 242 MWe with gas co-firing for meeting peak loads. Fuel pebbles are 30 mm diameter, much less than gas-cooled HTRs. A 410 MWe/900 MWt pebble bed version was also being designed with UC-Berkeley.
AHTR reactor sizes of 1500 MWe/3600 MWt are envisaged, with capital costs estimated at less than $1000/kW.
In the secondary cooling circuit, air is compressed, heated, flows through gas turbines producing electricity, enters a steam recovery boiler producing steam that produces additional electricity, and exits to the atmosphere. Added peak power can be produced by injecting natural gas (or hydrogen in the future) after nuclear heating of the compressed air to raise gas temperatures and plant output, giving it rapidly variable output (of great value in grid stability and for peak load demand where renewables have significant input). This is described as an air Brayton combined-cycle (ABCC) system in secondary circuit.
Moltex Energy LLP’s Stable Salt Reactor is a conceptual UK reactor design with no pumps (only small impellers in the secondary salt bath) and relies on convection from static vertical fuel tubes in the core to convey heat to the steam generators. Core temperature is 500-600°C, at atmospheric pressure. Decay heat is removed by natural air convection.
Fuel tubes of nickel-chromium alloy three-quarters filled with the molten fuel salt (60% NaCl, 40% Pu, U & lanthanide trichlorides) are grouped into fuel assemblies which are similar to those used in standard reactors and use similar structural materials. The individual fuel tubes are vented so that fission product gases escape into the coolant salt, which is a NaF-KF-ZrF4 mix (Li-7 fluoride is avoided for cost reasons). The assemblies can be moved laterally without removing them. Refuelling is thus continuous online, and after five years depleted assemblies are stored at one side of the pool pending reprocessing.
The primary fissile fuel in the original fast reactor version is plutonium-239 chloride with minor actinides and lanthanides recovered from LWR fuel or from its 'global workhorse reactor', though with 12% Pu quoted in one report. A 150 MWe pilot module is envisaged. It will have increased relevance if the UK government decides to commission it to help burn the UK's stockpile of plutonium. Commercial plants of 1000 MWe are envisaged. Overnight capital cost is estimated at about £1400 per kW.
The company then announced a ‘global workhorse' version of its design as 40 MWe modules running on LEU fluorides with "graphite built into the fuel assemblies" and thermal neutron spectrum.
A thorium breeder version will use thorium as a fuel source. In this, thorium is in the coolant salt and the U-233 produced is progressively dissolved in bismuth at the bottom of the salt pool. This contains U-238 to denature it. Once the desired level of U-233 is achieved, the bismuth with uranium is taken out batch-wise, and the mixed-isotope uranium is chlorinated to become fuel. If the fuel is used in a fast reactor, plutonium and actinides can be added.
The fuel assemblies are arranged at the centre of a tank half filled with the coolant salt which transfers heat away from the fuel assemblies to the peripheral steam generators, essentially by convection. The fuel assemblies are held in place by gravity in fittings set in the base of the tank, which is at atmospheric pressure.
Other liquid-fuel types: two-fluid breeders
Liquid Fluoride Thorium Reactor (LFTR)
The Liquid Fluoride Thorium Reactor (LFTR) is a heterogeneous MSR design which breeds its U-233 fuel from a fertile blanket of lithium-beryllium fluoride (FLiBe) salts with thorium fluoride. The thorium-232 captures neutrons from the reactor core to become protactinium-233, which decays (27-day half-life) to U-233. It may be possible to separate Pa-233 on-line and let it decay to U-233. Otherwise, newly-formed U-233 forms soluble uranium tetrafluoride (UF4), which is converted to gaseous uranium hexafluoride (UF6) by bubbling fluorine gas through the salt (which does not chemically affect the less-reactive thorium tetrafluoride). The volatile uranium hexafluoride is captured, reduced back to soluble UF4 by hydrogen gas, and finally is added to the FLiBe core to serve as fissile fuel. A complication is that traces of U-232 are formed, reporting with the U-233, and having highly gamma-active decay progeny.
LFTRs can rapidly change their power output, and hence be used for load-following. Because they are expected to be inexpensive to build and operate, 100 MWe LFTRs could be used as peak and back-up reserve power units.
Flibe Energy in the USA is studying a 40 MW two-fluid graphite-moderated thermal reactor concept based on the 1970s MSRE. It uses lithium fluoride/beryllium fluoride (FLiBe) salt as its primary coolant in both circuits. This is based on earlier US work on the molten salt reactor programme. Fuel is uranium-233 bred from thorium in FLiBe blanket salt. Fuel salt circulates through graphite logs. Secondary loop coolant salt is sodium-beryllium fluoride (BeF2-NaF). A 2 MWt pilot plant is envisaged, and eventually 2225 MWt commercial plants.
Other liquid-fuel types: single-fluid
Canada-based Terrestrial Energy Inc (TEI) has designed the Integral MSR. This simplified MSR integrates the primary reactor components, including primary heat exchangers to secondary clean salt circuit, in a sealed and replaceable core vessel that has a projected life of seven years. The IMSR will operate at 600-700°C, which can support many industrial process heat applications. It operates in the thermal neutron spectrum with a hexagonal arrangement of graphite elements forming the moderator. The fuel-salt is a eutectic of low-enriched (2-4%) uranium-235 fuel (as UF4) and a fluoride carrier salt – likely sodium rubidium fluoride with potential to change to FLiBe – at atmospheric pressure. Secondary loop coolant salt is ZrF4-KF. Multiple pumps and six heat exchangers allow for redundancy. Emergency cooling and residual heat removal are passive. When the sealed core is replaced after seven years, it is then left for fission products to decay. Each plant would have space for two reactors, allowing seven-year changeover, with the used unit removed for off-site reprocessing when it has cooled.
The IMSR is designed in three sizes: 80 MWth (32.5 MWe), 300 MWth, and 600 MWth. The total levelized cost of electricity from the largest is projected to be competitive with natural gas. The smallest is designed for off-grid, remote power applications, and as a prototype. The company expects to complete CNSC pre-licence review by the end of 2016, and hopes to commission its first commercial reactor by the early 2020s. In January 2015 the company announced a collaborative agreement with US Oak Ridge National Laboratory (ORNL) to advance the design.
Transatomic Power Corp is a new US company partly funded by Founders Fund and aiming to develop a single-fluid MSR using very low-enriched uranium fuel (1.8%) or the entire actinide component of used LWR fuel. The TAP reactor has an efficient zirconium hydride* moderator and a LiF-based fuel salt bearing the UF4 and actinides, hence a very compact core. The secondary coolant is FLiNaK salt (LiF-KF-NaF) to a steam generator.
Owing to the ZrH moderator, there are significantly more neutrons in the thermal region (less than 1 eV) compared with a graphite moderator, thereby enabling the reactor to generate power from very low-enriched uranium or used LWR fuel. The epithermal (1 eV - 1 MeV) spectrum is lower than that with graphite, but in the fast spectrum (over 1 MeV) the neutron flux is greater than with graphite moderator, and therefore contributes strongly to actinide burning. It would give up to 96% actinide burn-up. Fission products are mostly removed batch-wise and fresh fuel added. In addition to negative void and thermal coefficients, the moderator starts to fail at higher temperatures due to hydrogen loss. Decay heat removal can be by convection.
After a 20 MWt demonstration reactor, the envisaged first commercial plant will be 1250 MWt/550 MWe running at 44% thermal efficiency with 650°C in primary loop, using steam cycle. The overnight cost for an nth-of-a-kind 550 MWe plant, including lithium-7 inventory and on-line fission product removal and storage, is estimated at $2 billion with a three-year construction schedule. A version of the reactor may utilize thorium fuel.
The Fuji MSR is a 100-200 MWe graphite-moderated design to operate as a near-breeder and was being developed internationally by a Japanese, Russian and US consortium: the International Thorium Molten Salt Forum (ITMSF). It is based on the Oak Ridge MSBR, and several variants have been designed, including a 10 MWe mini Fuji. Thorium Tech Solutions Inc (TTS) plan to commercialise the Fuji concept, and is working on it with the Halden test reactor in Norway.
Martingale in the USA is designing the ThorCon MSR, which is a 250 MWe scaled-up Oak Ridge MSRE. It is a single-fluid thorium converter reactor in the thermal spectrum, graphite moderated. It uses a combination of U-233 from thorium and U-235 enriched from mined uranium. Fuel salt is sodium-beryllium fluoride (BeF2-NaF) with dissolved uranium and thorium tetrafluorides (Li-7 fluoride is avoided for cost reasons). Secondary loop coolant salt is also sodium-beryllium fluoride. It operates at 700°C. There is no on-line processing – this takes place in a centralized plant at the end of the core life, with off-gassing of some fission products meanwhile. A pilot plant would be similar to the mini Fuji.
Martingale aims for an operating prototype by 2020, with modular construction. Several 550 MWt units would comprise a power station, and a 1000 MWe Thorcon plant would comprise about 200 factory- or shipyard-build modules installed below grade (30 m down). All components are deigned to be easily and frequently replaced. For instance, every four years the entire primary loop would be changed out, returned to a centralized recycling facility, decontaminated, disassembled, inspected, and refurbished. Incipient problems would be rectified and major upgrades could be introduced without significantly disrupting power generation. The company claims generation costs of 3 to 5 c/kWh depending on scale, and is "targeting its first installations in forward-looking countries that support technology-neutral nuclear regulations and see the benefits of the license-by-test process."
Seaborg Waste Burner – SWaB
Seaborg Technologies in Denmark has a thermal-epithermal single fluid reactor design for 50 MWt pilot unit with a view to 250 MWt commercial modular units fuelled by spent LWR fuel and thorium. Fuel salt is Li-7 fluoride with thorium, plutonium and minor actinides as fluorides. This is pumped through the graphite column core and heat exchanger. Fission products are extracted on-line. Secondary coolant salt is FLiNaK, at 700°C. Spent LWR fuel would have the uranium extracted for recycle, leaving Pu and minor actinides to become part of the MSR fuel, with thorium.
Southern Co, MCFR
Southern Company Services in the USA is developing a molten chloride fast reactor (MCFR) with TerraPower, Oak Ridge National Laboratory (ORNL) – which hosts the work, the Electric Power Research Institute (EPRI) and Vanderbilt University. No details are available, and it is not certain that it is a single-fluid type. However, fuel is in the chloride salt (see section above) and as a fast reactor it can burn U-238, actinides and thorium as well as used light water reactor fuel, requiring no enrichment apart from initial fuel load (these details from TerraPower, not Southern).
In January 2016 the US DOE awarded a Gateway for Accelerated Innovation in Nuclear (GAIN) grant to the project, worth up to $40 million. In August 2016 Southern Nuclear Operating Company signed an agreement to work with X-energy to collaborate on development and commercialization of their respective small reactor designs. With TerraPower and ORNL, X-energy is designing the Xe-100 pebble-bed HTR of 48 MWe.
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