EP2612327A2 - Accelerator driven sub-critical core - Google Patents
Accelerator driven sub-critical coreInfo
- Publication number
- EP2612327A2 EP2612327A2 EP11822566.3A EP11822566A EP2612327A2 EP 2612327 A2 EP2612327 A2 EP 2612327A2 EP 11822566 A EP11822566 A EP 11822566A EP 2612327 A2 EP2612327 A2 EP 2612327A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- core
- vessel
- salt
- fission
- molten
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 230000004992 fission Effects 0.000 claims abstract description 105
- 238000000034 method Methods 0.000 claims abstract description 29
- 150000003839 salts Chemical class 0.000 claims description 135
- 239000000446 fuel Substances 0.000 claims description 80
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 43
- 150000002602 lanthanoids Chemical class 0.000 claims description 43
- 229910052768 actinide Inorganic materials 0.000 claims description 34
- 150000001255 actinides Chemical class 0.000 claims description 34
- 230000004907 flux Effects 0.000 claims description 33
- 230000005496 eutectics Effects 0.000 claims description 29
- 239000002915 spent fuel radioactive waste Substances 0.000 claims description 24
- 238000010248 power generation Methods 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 22
- 238000000605 extraction Methods 0.000 claims description 14
- 238000003860 storage Methods 0.000 claims description 14
- 238000004804 winding Methods 0.000 claims description 13
- 239000012530 fluid Substances 0.000 claims description 11
- 239000001307 helium Substances 0.000 claims description 9
- 229910052734 helium Inorganic materials 0.000 claims description 9
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 9
- 239000011833 salt mixture Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 229910052695 Americium Inorganic materials 0.000 claims description 4
- LXQXZNRPTYVCNG-UHFFFAOYSA-N americium atom Chemical compound [Am] LXQXZNRPTYVCNG-UHFFFAOYSA-N 0.000 claims description 4
- 230000008878 coupling Effects 0.000 claims description 4
- 238000010168 coupling process Methods 0.000 claims description 4
- 238000005859 coupling reaction Methods 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 4
- 230000002285 radioactive effect Effects 0.000 claims description 4
- 238000004821 distillation Methods 0.000 claims description 3
- 239000000284 extract Substances 0.000 claims description 3
- 239000003039 volatile agent Substances 0.000 claims description 3
- 239000012857 radioactive material Substances 0.000 claims description 2
- 239000011162 core material Substances 0.000 description 205
- 230000000712 assembly Effects 0.000 description 26
- 238000000429 assembly Methods 0.000 description 26
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 19
- 239000002245 particle Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 17
- 239000002699 waste material Substances 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 15
- OYEHPCDNVJXUIW-FTXFMUIASA-N 239Pu Chemical compound [239Pu] OYEHPCDNVJXUIW-FTXFMUIASA-N 0.000 description 13
- 229910052770 Uranium Inorganic materials 0.000 description 13
- 230000008569 process Effects 0.000 description 13
- 238000012546 transfer Methods 0.000 description 13
- 239000007788 liquid Substances 0.000 description 12
- 229910052776 Thorium Inorganic materials 0.000 description 11
- 238000002347 injection Methods 0.000 description 11
- 239000007924 injection Substances 0.000 description 11
- 229910052758 niobium Inorganic materials 0.000 description 9
- 239000010955 niobium Substances 0.000 description 9
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 9
- 238000009826 distribution Methods 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 7
- 230000001133 acceleration Effects 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- 239000002826 coolant Substances 0.000 description 6
- 238000010586 diagram Methods 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
- 238000009377 nuclear transmutation Methods 0.000 description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 238000005253 cladding Methods 0.000 description 5
- 239000012634 fragment Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- 229910052719 titanium Inorganic materials 0.000 description 5
- JFALSRSLKYAFGM-OIOBTWANSA-N uranium-235 Chemical compound [235U] JFALSRSLKYAFGM-OIOBTWANSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 230000005255 beta decay Effects 0.000 description 4
- 239000011449 brick Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000005684 electric field Effects 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 238000009395 breeding Methods 0.000 description 3
- 230000001488 breeding effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 239000011156 metal matrix composite Substances 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 230000005258 radioactive decay Effects 0.000 description 3
- 238000012958 reprocessing Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000002887 superconductor Substances 0.000 description 3
- 239000002914 transuranic radioactive waste Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910052781 Neptunium Inorganic materials 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002052 molecular layer Substances 0.000 description 2
- LFNLGNPSGWYGGD-UHFFFAOYSA-N neptunium atom Chemical compound [Np] LFNLGNPSGWYGGD-UHFFFAOYSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000005057 refrigeration Methods 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000008685 targeting Effects 0.000 description 2
- JFALSRSLKYAFGM-FTXFMUIASA-N uranium-233 Chemical compound [233U] JFALSRSLKYAFGM-FTXFMUIASA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910001275 Niobium-titanium Inorganic materials 0.000 description 1
- 229910052778 Plutonium Inorganic materials 0.000 description 1
- 150000001218 Thorium Chemical class 0.000 description 1
- 150000001224 Uranium Chemical class 0.000 description 1
- 229910001093 Zr alloy Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000000998 batch distillation Methods 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001944 continuous distillation Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- RJSRQTFBFAJJIL-UHFFFAOYSA-N niobium titanium Chemical compound [Ti].[Nb] RJSRQTFBFAJJIL-UHFFFAOYSA-N 0.000 description 1
- 229910000657 niobium-tin Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000010363 phase shift Effects 0.000 description 1
- OYEHPCDNVJXUIW-UHFFFAOYSA-N plutonium atom Chemical compound [Pu] OYEHPCDNVJXUIW-UHFFFAOYSA-N 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000002901 radioactive waste Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- SAWLVFKYPSYVBL-UHFFFAOYSA-K uranium(iii) chloride Chemical compound Cl[U](Cl)Cl SAWLVFKYPSYVBL-UHFFFAOYSA-K 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C1/00—Reactor types
- G21C1/30—Subcritical reactors ; Experimental reactors other than swimming-pool reactors or zero-energy reactors
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21G—CONVERSION OF CHEMICAL ELEMENTS; RADIOACTIVE SOURCES
- G21G1/00—Arrangements for converting chemical elements by electromagnetic radiation, corpuscular radiation or particle bombardment, e.g. producing radioactive isotopes
- G21G1/02—Arrangements for converting chemical elements by electromagnetic radiation, corpuscular radiation or particle bombardment, e.g. producing radioactive isotopes in nuclear reactors
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05H—PLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
- H05H13/00—Magnetic resonance accelerators; Cyclotrons
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C11/00—Shielding structurally associated with the reactor
- G21C11/06—Reflecting shields, i.e. for minimising loss of neutrons
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C11/00—Shielding structurally associated with the reactor
- G21C11/08—Thermal shields; Thermal linings, i.e. for dissipating heat from gamma radiation which would otherwise heat an outer biological shield ; Thermal insulation
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C3/00—Reactor fuel elements and their assemblies; Selection of substances for use as reactor fuel elements
- G21C3/42—Selection of substances for use as reactor fuel
- G21C3/44—Fluid or fluent reactor fuel
- G21C3/54—Fused salt, oxide or hydroxide compositions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E30/00—Energy generation of nuclear origin
- Y02E30/30—Nuclear fission reactors
Definitions
- the present disclosure is generally related to nuclear power generation, and more specifically related to generation of nuclear power using an accelerator driven sub-critical core.
- Generating power from nuclear fission utilizes a process in which fissionable nuclei of certain elements, for example uranium 235 ( 235 U), uranium 233 ( 233 U), or Plutonium 239 ( 239 Pu) undergo spontaneous fission or fission stimulated by absorption of a neutron.
- a nucleus splits into two smaller nuclei and a number of free neutrons.
- Neutrons produced in a fission event typically have large kinetic energy, typically of order MeV, and are called fast neutrons.
- a critical core typically includes fuel rods, or pins, containing fissionable nuclei. The fuel pins are arranged within a matrix of a material that decreases the kinetic energy of neutrons. This process is called moderation.
- a critical core is capable of self-sustained fission and is called a nuclear reactor.
- Stimulated fission of a 235 U nucleus has maximum probability for an incident neutron of low energy, typically of order eV, called a thermal neutron.
- Reactors using 235 U fission utilize low-atomic-weight materials, such as water or carbon, as moderators because fast neutrons scattering from such light nuclei quickly lose kinetic energy and become available to stimulate fission.
- the fuel pins and moderator in a conventional 235 U- fueled core are arranged so as to sustain an equilibrium in which just enough neutrons are produced in fission to stimulate more fission. Such an arrangement is called a critical pile.
- the condition of equilibrium must be stabilized by insertion or removal of additional rods of a material whose nuclei have large probability to capture neutrons (control rods).
- the insertion and removal of control rods can thus be used to maintain the neutron gain, or criticality, of the pile at the precise value of one; this situation is called a critical reaction. If too many neutrons are absorbed, the rate of fission decreases exponentially with time and the core shuts down. If too few neutrons are absorbed, the rate of fission increases exponentially with time and the core explodes.
- a critical fission core can be used to generate a large amount of heat, the heat used to generate steam, and the steam used to drive electric generators. Water- moderated 235 U-fueled fission reactors are commonly used to generate electric power.
- neutrons may be captured on certain heavy nuclei, for example uranium 238 ( 238 U) and thorium ( 232 Th), and through a sequence of such neutron capture and radioactive decay produce a fissionable nucleus such as 239 Pu (from 238 U) or 233 U (from 232 Th).
- This process is called breeding, and provides a mechanism by which the process of stimulated fission can actually produce additional fissionable nuclei within the core material
- minor actinides include neptunium (Np) and americium (Am).
- the minor actinides present a significant problem for safety of nuclear power, because they are produced in significant quantity in thermal reactors and they are the only elements that have radioactive decay half-life greater than a century and less than a million years.
- americium ( 241 Am) has a half-life of 432 years; 243 Am has a half-life of 7,370 years. For that reason they present a serious problem for disposal of spent nuclear fuel.
- a fission power generator includes a sub-critical core and a plurality of proton beam generators.
- Each of the proton beam generators is configured to concurrently provide a proton beam into a different area of the sub-critical core.
- Each proton beam scatters neutrons within the sub-critical core.
- the plurality of proton beam generators provides aggregate power to the sub-critical core, via the proton beams, to scatter neutrons sufficient to initiate fission in the sub-critical core.
- a method for reducing radioactive material includes injecting an externally produced minor actinide into a molten heavy salt eutectic core of a power generator. A plurality of proton beams is provided to the core. The minor actinide is split by fission in the molten heavy salt eutectic core.
- a sub-critical nuclear power generation system includes a molten salt eutectic core.
- the molten salt eutectic core includes an inner core vessel, a molten mixture of fuel salt and carrier salt, and a plurality of spallation targets disposed within the molten salt eutectic core. Each spallation target is arranged to receive a different proton beam.
- a method for extending the life of a nuclear core includes providing a molten mixture of fuel salt and carrier salt in the core.
- a lanthanide extraction system is coupled to the core.
- the molten mixture is provided to the lanthanide extraction system as the core operates.
- Lanthanides are separated from the molten mixture in the lanthanide extraction system to generate a purified salt mixture as the core operates.
- the purified salt mixture is provided to the core.
- Figure 1 shows a schematic diagram of a molten salt eutectic sub-critical core nuclear power generation system in accordance with various embodiments
- Figure 2 shows a schematic diagram of the molten salt eutectic core in accordance with various embodiments
- Figure 3 shows a top view of an isochronous cyclotron stack in accordance with various embodiments
- Figure 4 shows a perspective view of a flux-coupled isochronous cyclotron stack in accordance with various embodiments
- Figure 5A shows a view coil assemblies of a sector magnet of a flux-coupled isochronous cyclotron in accordance with various embodiments
- Figure 5B shows a cross-section view of the coil assemblies of a sector magnet of a flux-coupled isochronous cyclotron in accordance with various embodiments
- Figure 6 shows a cross-sectional view of a pair of coil assemblies 502 configured to produce alternating gradient quadrupole fields in accordance with various embodiments
- Figure 7 shows a top view of a cyclotron stack including strong focusing in accordance with various embodiments
- Figure 8 shows a schematic view of an RF cavity suitable for use a cyclotron stack in accordance with various embodiments
- Figure 9 shows a schematic view of an alternative RF cavity suitable for use with a stacked cyclotron in accordance with various embodiments
- Figure 10 shows a schematic view of a cross-section of an RF cavity 304 and associated magnetic shielding in accordance with various embodiments
- Figure 1 1 shows a schematic view of an alternative RF cavity including a single
- Figure 12 shows a schematic view of two RF cavities disposed between adjacent sector magnets in accordance with various embodiments
- Figure 13 shows a schematic diagram of a fuel pin based sub-critical core nuclear power generation system in accordance with various embodiments.
- Figure 14 illustrates overhead view of a proton beam distribution pattern in sub- critical nuclear core in accordance with various embodiments.
- Sub-critical cores contain fissionable fuel but they may be designed in a manner that they are incapable of a self-sustained fission chain reaction.
- fission is initiated and maintained by introducing fast neutrons into the core from an outside source.
- a particle accelerator can be used to generate fast neutrons by spallation. Spallation is a process wherein a collision between particles, e.g., an accelerated proton and a target nucleus, results in the ejection of multiple particles (primarily fast neutrons) from the target nucleus.
- particle accelerator induced fission in a sub-critical core may be referred to as Accelerator Driven Subcritical (ADS) fission.
- ADS Accelerator Driven Subcritical
- ADS fission addresses at least some of the aforementioned challenges of critical fission cores.
- ADS fission is directly controlled by the particle beam.
- ADS fission halts, providing direct control of the fission process.
- an ADS fission system may include sufficient thermal mass to preclude meltdown from radioactive heat after fission stops.
- ADS fission also provides greater flexibility for the composition and placement of fissile, fertile, or fission product waste within the core, and requires less enrichment of fissile content.
- ADS fission operates naturally in the fast neutron spectrum, rather than the thermal spectrum used by critical reactors.
- ADS fission systems are not without difficulties.
- CW continuous-wave
- MW megawatts
- Embodiments of the ADS fission systems of the present disclosure include features that overcome the deficiencies of critical cores and of conventional ADS systems which employ a single proton beam.
- Embodiments include multiple proton beam sources and multiple spallation targets. By incorporating multiple beams, embodiments generate the high beam power required to induce fission for power generation while also providing redundancy that enables core operation during beam interruption. Further, by dispersing the spallation targets about the core, core efficiency is enhanced and the need to reshuffle the fuel pins is reduced in those embodiments employing fuel pins.
- Some embodiments of the ADS fission system disclosed herein include a molten salt eutectic rather than fuel pins and moderator.
- the molten salt eutectic includes a mixture of fuel salt and carrier salt.
- a molten salt eutectic core there is no fuel pin cladding and no concerns related to cladding.
- the molten salt core provides a number of additional advantages over a core employing fuel pins. As explained above, an ADS core using fast neutronics can burn long-lived radioactive waste.
- the molten salt core provides fast neutronics and advantageously allows waste produced by conventional cores to be added to the fuel salt and destroyed.
- the molten salt core disclosed herein provides a means for destroying minor actinide waste produced by other sources, such as critical fission cores.
- the molten salt core can also be fueled with spent nuclear fuel in which fission products have accumulated to a degree that the fuel can no longer be used to generate fission in a critical fission core.
- the molten salt core allows for isolation and removal of fission products that absorb neutrons from the salt. Thus, embodiments are very efficient, allowing for complete or nearly complete consumption of all fertile fuel in the core. Furthermore, embodiments of the molten salt core herein disclosed provide fail-safe heat transfer. The core cannot melt through its containment even with a complete loss of power and coolant.
- FIG. 1 shows a molten salt eutectic sub-critical core nuclear power generation system 100 in accordance with various embodiments.
- the power generation system 100 includes a molten salt core 1 10, a particle accelerator complex 102, one or more primary heat exchangers 122, one or more secondary heat exchangers 1 12, and at least one turbine generator 1 14.
- Molten salt from or in the core 1 10 transfers heat to molten sodium, non-fuel salt, or another secondary fluid that is suitable to transport heat, in the primary heat exchanger 122.
- the heated fluid flows from the primary heat exchanger 122 to the secondary heat exchanger 1 12.
- heat provided by the fluid is used to generate steam, or another suitable pressurized fluid, that drives the turbine generator 1 14 to generate electrical power.
- the primary and secondary heat exchangers 122, 1 12 may be tube-and-shell heat exchangers as known in the art. Though only a single turbine generator 1 14 is shown, in practice, the system 100 may include more than one turbine generator 1 14.
- the power generation system 100 also includes a containment vessel 108, one or more lanthanide stills 120, a primary vessel 124, a set of conductive heat pipes 1 18, a lanthanide storage vessel 1 16, a volatile fission fragment storage vessel 126, and dump tanks 128.
- the lanthanide stills 120 and at least some portions of the primary heat exchangers 1 12 are contained within the primary vessel 124.
- the heat pipes 1 18 extend from the primary vessel 124 to a thermal sink.
- the primary vessel 124, lanthanide storage vessel 1 16, and volatile fission fragment storage vessel 126 are disposed within the containment vessel 108.
- the primary heat exchanger 122 is completely contained within the primary vessel 124 at a position above a neutron reflector 134.
- the molten salt 204 is isolated within the primary vessel 124.
- the flow of the molten salt 204 to the primary heat exchanger 122 is sustained by at least one pump and connecting pipes that transfer molten salt 204 from a plenum disposed at the upper levels of the molten salt 204 to an inlet of the primary heat exchanger 122.
- Embodiments of the primary heat exchanger 122 may transfer 400 MW of heat and be no more than about 2.5 meters in height, providing sufficient space to accommodate three or more particle beams entering the top of the primary vessel 124.
- the secondary fluid is circulated through the secondary tubing manifolds of the primary heat exchanger 122 by at least one pump and pipes connected to the secondary heat exchanger 1 12.
- Cooled molten salt 204 may flow from an outlet of the primary heat exchanger 122 to a cylindrical plenum shell forming an annulus just inside the side wall of the primary vessel 124.
- FIG. 2 shows a schematic diagram of the sub-critical molten salt eutectic core 1 10 and portions of the primary vessel 124 in accordance with various embodiments.
- the primary vessel 124 includes an inner core vessel 202 and an outer core vessel 210.
- the inner core vessel 202 contains the molten salt eutectic 204.
- the outer core vessel 210 is disposed about the inner core vessel 202, and separated from the inner core by space 208 and multi-layer radiant heat shield 206.
- the outer core vessel 210 includes a reflector 214 that contains neutrons within the core 1 10, thereby minimizing core leakage.
- the reflector may include lead.
- the outer core vessel 210 may include a lead filled stainless steel shell, and the walls of the outer core vessel 210 may be approximately .8 meters thick.
- the neutron shield 134 is disposed above the molten salt 204 to isolate components, such as the primary heat exchanger 122 and lanthanide still 120, from the core neutronics.
- the neutron shield 134 may also comprise lead.
- the core 1 10 generate approximately 400 megawatts (MW) of heat, and the molten salt has a temperature of 600°-800° Celsius while the outer core vessel 210 operates at about room temperature.
- the space 208 between the inner core vessel 202 and the outer core vessel 210 is void of fluid (in a state of vacuum) when the core 1 10 is operating.
- the vacuum and the multi-layer heat shield 206 serve to inhibit conduction and/or radiation of heat from the inner core vessel 202 to the outer core vessel 210. In some embodiments, the vacuum and the multi-layer heat shield 206 limit the heat transferred from the inner core vessel 202 to the outer core vessel 210 to less than about 1 MW.
- the space 208 also serves as a component of a safety subsystem of the system 100. Under conditions in which heat transfer from the molten salt 204 is inhibited, for example, a failure of the heat exchangers 122, 1 12, the space 208 may be filled with a fluid that facilitates conduction of heat from the inner core vessel 202 to the outer core vessel 210. Such a condition may occur, for example, if power is lost to the heat exchangers 122, 1 12. Under such conditions, fission and heating caused by fission are discontinued, but decay of fission products within the molten salt 204 continues to generate heat in the core 1 10 for a time.
- heat conduction between the core vessels 202 and 210 is provided by filling the space 208 with helium gas.
- the helium may be at atmospheric pressure.
- embodiments of the system 100 may include a helium source activated manually or automatically to fill the space 208 when thermal energy is to be conducted from the inner core vessel 202 to the outer core vessel 210.
- another thermally conductive fluid may be used in place of or in addition to helium.
- the conductive heat pipes 1 18 may be fluid filled and operate to conduct heat away from the outer core vessel 210 to heat dissipation structures, such as radiator panels or a geothermal heat sink. Because the molten salt 204 is in direct and constant contact with the surface of the inner core vessel 202, heat transfer from the salt 204 to the inner core vessel 202 is uninhibited. Thus, the molten salt eutectic 204 in combination with the described heat transfer features greatly enhance overall safety of the system 100 relative to conventional critical cores by making core meltdown extremely unlikely or impossible.
- the molten salt eutectic 204 contained within the inner core vessel 202 includes a carrier salt and a fuel salt.
- the carrier salt may be NaCI and/or another suitable heavy salt. Some embodiments may use lithium salts or potassium salts.
- the carrier salt features relatively heavy atomic weight nuclides that contribute to the fast neutronics of the core 1 10 by maintaining neutron energy in the MeV range as neutrons collide with the carrier salt nuclei. In contrast, light salts and other light materials cause reduction of neutron energy on collision.
- the fuel salt may be, for example, a uranium salt including the same halide (chlorine, fluorine, bromine, etc.) as the carrier salt (e.g., uranium trichloride).
- the neutron gain of the molten salt 204 is less than one (between .85 and .97 for example), and the salt mixture is consequently incapable of self-sustained fission.
- the neutrons required to initiate and sustain fission are provided via spallation.
- the core 1 10 includes an array of spallation targets 212.
- Each spallation target 212 includes one or more metal plates.
- the metal plates are formed of a tough and ductile material, such as tungsten, and may be about 1 centimeter thick or more.
- a beam of energetic protons is guided to each spallation target 212, via an evacuated vacuum tube, from the particle accelerator complex 102.
- each proton liberates approximately twenty neutrons.
- the liberated neutrons collide with the nuclei of the fuel salt to initiate fission.
- the spallation targets 212 are arranged symmetrically around the center of the inner core vessel 202 in a roughly circular pattern (e.g., see Fig. 14 for an exemplary arrangement of seven spallation targets). In some embodiments, the pattern may have a radius that is approximately 1/3 of the radius of the inner core vessel 202.
- Each spallation target 212 is driven with a proton beam generated by a different particle accelerator of the accelerator complex 102.
- embodiments of the system 100 allow the core 1 10 to be driven with high aggregate beam power while employing accelerators that provide modest beam power.
- the multiple targets 212 and associated accelerators of the accelerator complex 102 also provide a level of redundancy, wherein failure of one accelerator does not shut down the core 1 10. Instead, embodiments of the system 100 can continue to operate, at a reduced power level, when one or more particle accelerators are inoperative.
- the multiple proton beams enhance the efficiency of the core 1 10.
- the fast neutronics provided by the heavy molten salt 204 allows the core 1 10 to breed fuel from non-fissile materials such as thorium, uranium 238 ( 238 U), etc. Via the process of transmutation wherein non-fissile nuclei capture neutrons in the core 1 10 and undergo radioactive decay, non-fissile materials can be transmuted into fissile materials such as uranium 233 or plutonium 239.
- the fuel cycle for 238 U involves transmuting 238 U to 239 U by neutron capture followed by beta decay to neptunium and plutonium 239.
- the ultra-fast neutronics of the molten salt 204 also allows for fission of long- lived waste isotopes that are generated in the core 1 10.
- Waste materials e.g., minor actinides, such as americium
- long half-lives e.g., 1 -10,000 years
- the core 1 10 is configured to maintain an equilibrium level of minor actinides, the core 1 10 can be used to consume waste actinides produced by conventional cores, thereby reducing or eliminating the need to store the actinides and the attendant security concerns. Minor actinides or other waste generated by a conventional core can be periodically added to the molten salt 204 and consumed. Thus, the core 1 10 provides a method for destroying dangerous waste that would otherwise require secure storage.
- Spent nuclear fuel contains a large quantity of the fertile nuclide 238 U, modest quantities of the fissile nuclides 235 U and 239 Pu, and a significant quantity of minor actinides.
- the power generation system 100 can be used to maintain an equilibrium in which the fertile nuclide 238 U is transmuted into the fissile isotope 239 Pu, and the 239 Pu is fissioned, so that the inventory of 239 Pu remains roughly constant while the 238 U is consumed. This equilibrium is called isobreeding, and makes it possible for the power generation system 100 to extract most of the available energy from the spent nuclear fuel.
- the process of transmutation also breeds a portion of the 238 U into heavier nuclides, including the minor actinides.
- the probability for fission of the minor actinides is as great as the probability for breeding them, so the inventory of minor actinides does not continue to increase during the isobreeding cycle but reaches and remains at an equilibrium inventory.
- some embodiments of the molten salt core 1 10 use thorium as the fertile nuclide in the molten salt 204.
- the low atomic weight of thorium maximizes the number of neutron captures required to breed minor actinides.
- the stable nuclide 232 Th is 9 atomic mass units lighter than the minor actinide 241 Am, and so it requires the capture of 9 fast neutrons in order to breed 232 Th into 241 Am, whereas it requires only 3 neutron captures to breed 238 U into 241 Am.
- a thorium-fueled power generation system 100 has a much smaller equilibrium inventory of minor actinides than a uranium fueled system, and therefore may be used as an incinerator for minor actinides that had been produced in the operation of conventional fission power plants.
- use of thorium rather than uranium in the molten salt 204 may reduce minor actinide inventory in the core 1 10 by a factor of 10 4 .
- Minor actinides from spent nuclear fuel may be separated chemically, and the separated minor actinides added periodically to the fuel salt 204 of an operating power generation system 100. The added minor actinides are consumed by fission, and the inventory of minor actinides would return to its equilibrium value, essentially without limit.
- spent fuel pins may be disposed in the molten salt 204 to raise the initial neutron gain of the core 1 10.
- isobreeding raises the neutron gain of the molten salt 204 to a level sufficient to provide high core efficiency.
- the solubility of fuel salt (e.g. UCI3) in the carrier salt may limit the molten salt 204 to a relatively low neutron gain (e.g., .7), which corresponding limits the initial efficiency of the core 1 10.
- the initial neutron gain of the molten salt 204 may be enhanced by addition of enriched uranium to the molten salt 204.
- enriched uranium may raise security concerns.
- the core 1 10 may advantageously include spent fuel pin assemblies removed from a conventional thermal core to raise the initial neutron gain of the core 1 10.
- the spent fuel pin assemblies may be symmetrically arranged in the core 1 10.
- the spent fuel pin assemblies may be disposed about the perimeter of the primary vessel 122 in cooled molten salt 204 flowing in the annulus formed between the wall of the primary vessel 124 and the cylindrical plenum shell coupled to the output of the primary heat exchanger 122.
- embodiments of the core 1 10 may raise initial neutron gain to about .95 or higher without use of enriched uranium.
- fuel salt extracted from spent nuclear fuel provides fissile content sufficient for efficient operation of the core 1 10 from startup. In such embodiments, enrichment may not be required.
- An embodiment of the core 1 10 may include about 30 tons of uranium in the molten salt 204 and may generate 400 MW of continuously for 100 years or more.
- the uranium and other fertile and fissile components of the molten salt 204 may be extracted from spent nuclear fuel generated by a conventional reactor.
- the spent fuel produced by a conventional reactor may require removal and replacement at about five year intervals.
- the spent fuel contains about 80 tons of uranium and 328 kilograms of 239 Pu, and may be processed using the Experimental Breeder Reactor-ll (EBR2) reprocessing technology to generate the fuel salt used by the core 1 10.
- EBR2 Experimental Breeder Reactor-ll
- EBR2 reprocessing extracts the fuel from the fuel assemblies of spent nuclear into molten salt, and then deposits metallic uranium by electro-separation leaving all other components in the salt.
- Thirty tons of spent nuclear fuel may be processed through only the first stage of the EBR2 process to produce salt containing all the uranium and transuranic waste (TRU) of the spent fuel.
- the salt extracted from the thirty tons of spent fuel contains about 123 kg of 239 Pu.
- Another 420 tons of spent fuel may be processed through the full EBR2 process to extract the spent fuel into salt followed by separation of metallic uranium from TRU salt.
- the remnant salt contains about 4590 kilograms of 239 Pu.
- the remnant salt may be combined with the salt produced from the initial 30 tons of spent fuel to produce the fuel salt for the core 1 10.
- the fuel salt produced by combining the salts includes about 4.71 tons of 239 Pu and 30 tons of uranium, corresponding to a fissile content of about 13%. The remaining 415 tons of metallic uranium is available for other uses.
- the amount of spent fuel reprocessed as described above is equivalent to about six five-year fuel cycles of a conventional reactor, and such amount may be available at any number of nuclear power generation sites. Consequently, an instance of the power generation system 100 may be co-located with a conventional reactor that provides the fuel for the core 1 10.
- the power generation system 100 is configured to purify the molten salt 204 as the system 100 operates.
- the lanthanide stills 120 disposed in the primary vessel 124 extract lanthanides from the molten salt 204 while the core 1 10 is in operation.
- the extracted lanthanides are stored in the lanthanide storage vessel 1 16.
- Lanthanides are fission products that build up the molten salt 204 during system operation.
- the lanthanides have relatively large cross sections for absorbing the neutrons propagating within the core 1 10. Consequently, the build-up of lanthanides in the molten salt 204 makes neutrons unavailable for fission, and is therefore detrimental to the efficiency of the core 1 10.
- the build-up of lanthanides in the fuel pins necessitates shuffling and/or premature replacement of the pins.
- Embodiments of the power generation system 100 maintain high efficiency by extracting lanthanides from the molten salt 204 while the core 1 10 operates.
- the vapor pressure versus temperature of the lanthanides is about 100 times lower than that of the fuel salts (actinides). Consequently, the fuel salts can be separated from the lanthanides via heating and distillation in the lanthanide stills 120.
- the lanthanide stills 120 include heating elements that heat the molten salt 204 to a temperature that vaporizes the fuel and carrier salts, leaving the lanthanides.
- the vaporized salts are condensed using cooled molten salt 204 and returned to the core 1 10.
- the lanthanides are accumulated and stored in the lanthanide storage vessel 1 16 for removal when the core 1 10 removed from service. Removal of lanthanides from the molten salt 204 improves the efficiency of the core 1 10, and extends the useful life of the core 1 10 by allowing for the fuel salt to be more completely consumed. Furthermore, the extracted lanthanides are valuable rare- earth elements that can be recycled to produce various products.
- Some lanthanide stills 120 employed in the system 100 utilize a batch distillation process. In the batch process, a quantity of molten salt 204 is processed at a periodic interval. Other embodiments of the lanthanide stills 120 employ a continuous distillation process. In the continuous process, molten salt 204 is constantly refined.
- Some embodiments of the system 100 include one or more cryotraps for removing volatiles (such as krypton and xenon) created in the core 1 10. Gases are condensed in the cryotraps and stored in the volatile fission fragment storage vessel 126 for removal when the core is decommissioned. Some embodiments of the system 100 provide a stream of inert gas, such as helium, in the inner core vessel 202 to sweep volatiles into the cryotraps for extraction.
- volatiles such as krypton and xenon
- each spallation target 212 of the core 1 10 is associated with a proton beam generated by the accelerator complex 102.
- the accelerator complex 102 includes a plurality of particle accelerators to generate the proton beams.
- the accelerator complex 102 may include a different particle accelerator for each spallation target 212.
- Some embodiments of the accelerator complex 102 include isochronous cyclotrons serving as the particle accelerators.
- the accelerator complex 102 also includes an injector 132.
- the injector 132 may produce a single proton beam or multiple proton beams. In some embodiments, the injector 132 may produce proton beams at kinetic energy in the range from 70 MeV to 200 MeV traveling at approximately one-third the speed of light.
- the cyclotron stack 130 may accelerate the proton beams before they reach the spallation targets 212.
- each proton beam generated by an isochronous cyclotron of the accelerator complex 102 may produce an average of about 2 milliamps of current and 700MeV.
- the protons beams provided to the core 1 10 may, in aggregate, provide about 10 MW or more of beam energy.
- the isochronous cyclotrons of the accelerator complex 102 may be arranged as a cyclotron stack 130.
- the cyclotrons of the cyclotron stack 130 are independently operating isochronous cyclotrons, and are arranged in a flux-coupled vertical stack with minimal separation between cyclotrons.
- the vertical stacking allows the multiple cyclotrons to share a footprint approximately corresponding to that of a single cyclotron.
- embodiments of the accelerator complex 102 consume less space and are more economical than a corresponding number of convention particle accelerators.
- the cyclotrons share magnetic flux return while other subsystems (RF cavities, insertion, extraction, etc.) are independent, allowing continued operation of one cyclotron if another cyclotron fails.
- Each cyclotron of cyclotron stack 130 generates one of the multiple proton beams used to drive the fission in core 1 10. Cumulatively, the accelerated beams from cyclotron stack 130 provide the beam current and/or energy to stimulate fission. Because no single beam is required to produce the desired amount of beam current and/or energy, core 1 10 may continue to operate even after one or more of the cyclotrons cease to operate. Moreover, using multiple proton beams alleviates the need to design a particle accelerator capable of producing a single beam with the desired level of beam current and energy.
- the cyclotron stack 130 includes a magnetic ring containing a plurality of similar sector magnets, RF accelerating cavities, injection accelerator and injection channel, extraction channel, and beam transport to an injection channel on the core 1 10.
- the sector magnets and RF cavities of cyclotron stack 130 operate to accelerate the proton beams provided from injector 132. As the proton beams circle the cyclotron stack 130 they gain speed and energy causing the protons in the proton beam to move in a spiral pattern. As the protons reach their desired energy, they are ejected from cyclotron stack 130 and directed to core 1 10 of system 100 to initiate fission.
- FIG. 3 shows a top view of the isochronous cyclotron stack 130 in accordance with various embodiments.
- the cyclotron stack 130 includes a plurality (e.g., seven) vertically stacked cyclotrons.
- Each cyclotron may be able to receive a low energy proton beam 306 in a circular orbit in the inner radial region of the cyclotron which is accelerated before being directed to the core 1 10.
- the proton beam within each cyclotron may circulate in a relatively flat cylindrical vacuum tank enclosed within the gaps 308 of a symmetrical arrangement of magnetic dipole sector magnets 302.
- Each cyclotron of the cyclotron stack 130 may include fewer RF cavities 304 than sector magnets 302.
- the sector magnets 302 may comprise superferric fields in which the magnetic field produced is limited to less than what would saturate the steel in its flux return (e.g., approximately 1 .8 T).
- the RF frequency of operation of the RF cavities 304 may be based on the revolution frequency of the proton beam in the cyclotron (e.g., about 50 MHz which corresponds to harmonic 8 of the revolution frequency in 1 .8 Tesla guide field).
- the RF cavities 304 may be superconducting RF cavities or dielectric-loaded superconducting RF cavities. In certain embodiments, the RF cavities 304 may be configured as a half-wave structure or as a shorted transmission line. The RF cavities 304 occupy less space than conventional RF cavities.
- each proton bunch gains kinetic energy it spirals towards the outer radial region of cyclotron stack 130.
- the pole geometry of sector magnets 302 may be designed so that the average bending field yields a constant orbit frequency even as the proton energy becomes comparable to its rest mass energy. This may allow synchronism with the RF field to be maintained.
- an extraction septum electrode 310 may be situated to outwardly deflect the outermost proton orbit so that it can be extracted into a beam transport line coupled to the core 1 10.
- the frequency of the RF field generated by the RF cavities 304 may be synchronous with an integral harmonic of the orbit frequency of the protons, thereby accelerating the protons by the cavity voltage V on each revolution of the proton orbit.
- the spiraling orbits of the accelerating protons may be spaced so as to increase the efficiency of extraction of a high-current beam at, for example, 800 MeV.
- this spacing may be facilitated by providing a relatively high RF voltage V (e.g., a total of 1 MeV energy gain per turn of orbit).
- the spacing may be further facilitated by using a relatively low magnetic field (e.g., less than 1 .8T) so the radial separation from a given energy gain per turn is maximized.
- Figure 4 is a perspective view of the flux-coupled isochronous cyclotron stack 130 in accordance with particular embodiments.
- Sector magnet 302A is shown in isolation.
- the cyclotron stack 130 includes seven isochronous cyclotrons arranged in a vertical stack.
- Other embodiment of the cyclotron stack 103 may include a different number of cyclotrons.
- Figures 5A shows a perspective view of coil assemblies 502 of the sector magnet 302 in accordance with various embodiments.
- Figure 5B shows a cross-sectional view of coil assemblies 502 of the sector magnet 302 in accordance with various embodiments.
- Sector magnet 302 includes a plurality of coil assemblies 502 (shown as 502A-H) which are supported in a vertical stack with vacuum gaps 504 between adjacent pairs of coil assemblies 502. The magnetic field for each cyclotron is generated by an adjacent pair of coil assemblies 502.
- Each coil assembly 502 consists of one or more superconducting windings 508 bonded to a magnetically permeable steel flux plate 506.
- the superconducting windings may be niobium-titanium alloy.
- the vacuum gap 504 between each adjacent pair of coil assemblies 502 constitutes the aperture through which one proton beam circulates as it is accelerated in the respective cyclotron.
- the sector magnets 302 include eight coil assemblies 502 defining seven apertures (i.e., seven isochronous cyclotrons).
- the entire stack of coil assemblies 502 for sector magnet 302 is supported within the aperture of a C-shaped flux return 510 made of magnetically permeable steel. Magnetic flux passes from one gap 504 to the next and is returned through the single C-shaped room-temperature steel flux return 510 facilitated by flux plate 506.
- coil assemblies 502 may be maintained at the cryogenic temperature of liquid helium, while the surrounding C-shaped flux return 510 is maintained at room temperature.
- the balancing may be attained by appropriate design of the geometry of the superconducting winding assembly 508 and the succession of vacuum gaps 504 between them in the stack. This may have the benefit that the Lorentz forces, which can be immense in comparison to the gravitational weight of the segments, are held in balance one with the next.
- the Lorentz forces from coil assembly 502C pulling up on coil assembly 502D may be approximately equal to the Lorentz forces from coil assembly 502E pulling down on coil assembly 502D. This balance may be attained with relatively little or no impact upon the magnetic field distribution in gaps 504.
- the tension support members 512 that support the stack of cryogenically cooled coil assemblies 502 within the room-temperature flux return 510 therefore may only need to support the gravitational weight of the elements, and not the much larger Lorentz forces. This may allow for the support of the huge Lorentz forces with a structure that would not be a thermal short between the 4K coil assembly and the warm-iron flux return. This benefit permits design of tension supports 512 allowing a reasonable minimum of conductive heat load through the supports 512.
- the coil assemblies 502 are configured to produce alternating gradient quadrupole fields.
- the coil assemblies 502 generate an array of quadrupoles, one quadrupole centered on the equilibrium orbit of each consecutive beam orbit.
- the quadrupoles focus the proton beam to direct the beam along the equilibrium orbit of each turn in the cyclotron.
- embodiments of the accelerator stack 130 require less calibration, setup, and maintenance than other cyclotrons, have larger acceptance of the beam phase space, and permit acceleration of larger beam current with smaller losses, making embodiments more suitable for industrial use.
- Figure 6 shows a cross-sectional view of a pair of coil assemblies 502 configured to produce alternating gradient quadrupole fields.
- the face of the coil assembly 502 includes a set of triangular or sawtooth ridges 602 that produce the quadrupoles defining the orbits 606 of the proton beam.
- the face of the coil assembly 502 includes pole-face winding 604 that that produce the quadrupoles.
- Yet other embodiments include ridges 602 and pole-face windings 604.
- Other embodiments of the coil assembly 502 may include different shaped ridges and produce a different field, e.g., an octupole field.
- Figure 6 also shows magnetic field distribution in the gap between coil assemblies 502 equipped with both a ridged steel surface 602 and pole-face windings
- the quadrupole gradient produced by the ridges 802 alone is G -1 .5 T/m.
- the quadrupole gradient produced by the pole face winding 604 alone, excited with 1000 A/mm 2 in a 1 mm thick winding, is
- the quadrupole gradient produced by the combination of ridges 602 and windings 604 together is G-2.5 T/m, corresponding to a focal length for focusing the proton beam, as it passes through the sector dipole, of
- Some embodiments of the accelerator stack 130 configure the quadrupoles on successive sector magnets 302 to have alternating-sign gradient for each orbit; this produces a focus/defocus (FODO) alternating-gradient focal channel with transport beta function comparable to the focal length ⁇ ⁇ f, and betatron tunes ⁇ 2nRi ⁇ 10.
- FODO focus/defocus
- embodiments of the accelerator stack 130 produce strong-focusing transport of the proton beam within the orbits of the each isochronous cyclotron using the pole-face quadrupoles described above.
- the strong-focusing beam transport provides embodiments of the accelerator stack 130 with a number of advantages.
- embodiments can make the tuning the same for all orbits, and can be used to select a tuning value that avoids fractional resonances and coupling resonances.
- the transverse size of the beam is inversely proportional to ⁇ , the beam size may be reduced by a factor of two or more compared to a conventional weak-focusing transport.
- embodiments of the accelerator stack 130 provide ample focusing using the pole face method disclosed above and may employ uncurved sector magnets.
- Figure 7 shows a top view of a cyclotron stack 700 including pole faces configured to generate a quadrupole gradient as described above.
- the sector magnets 702 include uncurved sides 704 that facilitate placement of the RF cavities 704.
- the cyclotron stack 700 may be substituted for the cyclotron stack 130 in embodiments of the accelerator complex 102.
- the cyclotron stack 130 arranges a plurality of cyclotrons in close proximity to one another.
- cyclotron spacing in the sector magnet 302 may be approximately .35 meters or less.
- Embodiments of the cyclotron stack 130 include RF cavities 304 configured to operate within such dimensions.
- Figure 8 shows a schematic diagram of a cutaway side view of an RF cavity 304 suitable for use with the cyclotron stack 130 in accordance with various embodiments.
- the RF cavity 304 comprises two RF chambers 802 and 804.
- RF chambers 802, 804 may be arranged symmetrically above and below the acceleration gap 806.
- RF chambers 802, 804 may be oriented parallel to the acceleration gap 806 (disposed in horizontal planes or planes parallel to the orbitary plane of the cyclotron) as shown. This arrangement may produce a symmetric pattern of accelerating electric fields in the region traversed by the proton beam. Such an above/below configuration may allow the half-wave or shorted stub-line geometry to be terminated at the innermost and outermost extent of the radial region bracketed by the cavity 304.
- the RF cavity 304 is continuous and wraps on itself at both the inner (not shown) and outer end 808) of the cavity 304 to reduce or eliminate coupling to longitudinal modes for which the electric field is oriented to point towards or away from the center of the cyclotron.
- RF signal is coupled to the cavity 304 at points 810 at the far end of the chambers 802, 804.
- the system 100 may include solid state power amplifiers to drive the RF signal to the RF cavity 304.
- one or more solid state RF power amplifier may be configured to drive RF signal to each point 810.
- the multiple power amplifiers provide redundancy and allow the cavity 302 to continue to operate should one or more power amplifiers fail. Multiple amplifiers may be used to introduce RF power in the same distribution in radius as the distribution of power that is delivered by the cavity to the successive orbits of proton beam, so that the currents on the cavity walls flow purely in the desired accelerating mode.
- the walls of RF cavity 304 may be made from a superconducting material, such as niobium or other suitable superconductor, and refrigerated to a temperature suitable for superconducting operation.
- the RF cavity 304 may operate at the 4 th or 6 th harmonic of the revolution frequency of the protons' orbit through the cyclotron.
- the RF cavity 304 may be capable of 1 MV accelerating voltage and excellent mode stability.
- FIG. 9 shows another embodiment of an RF cavity 904 suitable for use with the accelerator stack 130.
- the alternate cavity 904 includes horizontal chambers 906, 908.
- the RF cavity 904 may comprise a shorted transmission line containing a high-permittivity dielectric slab 910.
- the dielectric slab 910 may comprise rutile (a-phase T12O3) or another suitable material.
- the walls 912 of RF cavity 904 may be made from a superconducting material, such as niobium or other suitable superconductor.
- the surface field may be kept within breakdown limits by providing slot space between the superconducting walls of RF cavity 904 and dielectric slab 910, and by tapering the width of the slot space so that the electric field in the slot space is made approximately constant throughout RF cavity 904.
- the predominant share of RF losses may occur in dielectric slab 910. Maintaining dielectric slab 910 at a higher operating temperature than that of the superconducting walls 912 may improve the Carnot-cycle efficiency with which the heat from RF losses may be pumped to room temperature.
- dielectric slab 910 within RF cavity 904 may be suspended clear of the walls 912 within the above-mentioned slot space. The walls 912 and dielectric slab 910 may be refrigerated at different temperatures.
- the walls 912 may be refrigerated at approximately 4 K (the temperature of liquid helium, needed to sustain superconducting operation) and dielectric slab 910 at 20 K (using LNe coolant) or 80 K (using LN 2 coolant) to minimize loss tangent of the dielectric 910.
- Other, more advanced superconducting materials such as Nb3Sn, may be used as a surface coating on the inner surface of the niobium cavity. This may permit operation at a higher temperature than with pure niobium, such as 8-12 K. The increase in temperature may improve the Carnot-cycle efficiency with which the heat from RF losses may be pumped to room temperature.
- RF cavity 904 may comprise a pattern of azimuthally oriented slots in the superconducting walls 912 to mode-lock the cavity 904 so that the fields and currents within the RF cavity 904 are maintained in the mode appropriate for its acceleration of proton bunches circulating in the beam.
- This form of mode selection may permit stabilization of the cavity 904 against distortions in the fields that would arise from beam loading, from power coupling, and/or from termination of the cavity structure at the outermost and innermost radial extent of each RF cavity 904.
- the height of the dielectric 910 may be determined using the equation
- the relative permittivity ⁇ of the material is 125 (the average value for rutile at room temperature)
- the target frequency / is 48 MHz
- the speed of light c is 3x10 8
- the height L of the dielectric is:
- Increasing the length of RF cavity 904 may reduce the amount of dielectric used, increase the insulating gap, and reduce the peak field in the structure.
- Dielectric 910 may be recessed within RF chamber so that there is no line of sight from the proton beam as it passes through acceleration gap 914 (e.g., non-linear dynamical effects, inverse Cerenkov, etc). This may help to prevent a variety of secondary field interactions and charging phenomena that can limit high-current operation.
- dielectric 910 may be separated from the walls of RF cavity 904 by a vacuum gap for thermal isolation.
- dielectric 910 may be supported in RF chambers 906, 908 via a pattern of rutile tubes that pass through cut-off holes in the walls of RF cavity 904. The rutile tubes may then be refrigerated with a forced flow of liquid nitrogen at 80K. This may allow for approximately 1 MV of accelerating voltage.
- dielectric 910 may comprise fusion- bonded bricks wherein milled side faces form LN 2 coolant slots.
- the geometric factor of RF chambers 906, 908 may be 4.25 W as determined from the equation
- the surface resistance of the niobium at 4.2 K is determined by residual resistance of the bulk niobium, which for cavity-grade niobium is less than 10 ⁇ .
- the power dissipated on the niobium walls, at 4.2 K, 48 MHz, may be about 10 nW.
- the integral ⁇ H 2 ds is 2.1 A 2 /m (for 25.2 V across gap), corresponding to a wall dissipation of 33 W/m in the niobium for the full-geometry cavity. For a stack of 5 cyclotrons, each containing four 5-m-long cavities, this would constitute a cryogenic heat load of 3.5 kW at 4.2 K, equivalent to a mains power requirement of approximately 3 MW for refrigeration.
- the Q-value of the cavity 904 may be about 3.3x10 7 , with losses of 33 W/m (at 4.2K) for the superconducting walls 912 of RF chamber 908, 906 and 1 .2kW/m (at 77K) for dielectric 910.
- the shunt impedance of the dielectric-loaded shorted-stub cavity 904 may be
- Losses from the walls 912 of RF cavity 904 may be about 250 W/m. Radiation heat load from a warmer dielectric may bring another 1 1 W/m. The total heat load on liquid helium refrigeration system may be about 261 W/m. In certain instances, a magnetic field on the walls of RF cavity 904 may be approximately 1600 Oe.
- dielectric 910 may be assembled from identical square-cross-section dielectric bricks in which one side face may be milled to form a rectangular pocket.
- the bricks may be fusion-bonded to seal the pocket channels so that they provide flow channels for coolant to flow.
- the brick size may provide sufficient surface heat transfer to keep within the 1 W/cm 2 limit that is typical for the transfer to liquid coolant to avoid boiling.
- the thickness of dielectric 910 may be tapered. This may help to maintain a roughly constant electric field level along acceleration gap 914. Accelerating voltage with no phase shift is defined as
- w is an angular frequency
- v is a speed of the particle
- the ends of RF cavity 904 may be terminated by continuing the superconducting walls around a U-turn beyond the region traversed by the proton beams. This may connect one cyclotron layer to the next.
- Another method for terminating the ends of RF cavity 904 may be to continue the superconducting wall of RF chambers 906, 908 without continuing dielectric 910.
- the superconducting wall 912 may extend with a logarithmic taper of the inner vertical separation. In both methods the magnetic fields can be maintained with little perturbation over the portion of acceleration gap 914 traversed by the proton beams.
- Figure 10 shows a cross-sectional view of an RF cavity 304 and associated magnetic shielding 1002 in accordance with various embodiments.
- the accelerator complex 102 includes magnetic shielding 1002 disposed between each RF cavity 304 and adjacent sector magnet 302 in accordance with various embodiments.
- the arrangement of coil assemblies 502 produces a pattern of magnetic flux that primarily flows between adjacent coil assemblies 502. However, some of the magnetic flux may fringe into the regions flanking the sector magnet 302.
- the RF cavity 304 is positioned between sector magnets 302.
- the magnetic shielding 1002 shields the RF cavity 304 from the magnetic field produced by the coil assemblies 502 thereby preventing the magnetic field from saturating the superconductor of the cavity 304 and rendering the cavity 304 inoperable.
- the magnetic shielding 1002 includes a plurality of metal plates 1004.
- the metal plates 1004 may be made from permeable steel, or from high-permeability alloy. Each plate 1004 extends vertically nearly to the plane of beam orbits, and is disposed to intercept fringe flux and conduct the flux back to the flux plate 506, thereby closing the flux path. Each plate 1004 connects to a horizontal plate segment that connects from the end of the plate farthest from the beam plane to the side wall of the flux plate 506. By creating a low-reluctance path for fringing magnetic flux, the level of flux reaching the cavity 304 is greatly reduced. A succession of multiple plates 1004 may be placed in this manner, with a gap space between successive plates 1004, to optimize shielding of the fringe field. For, example two plates 1004, may be disposed with suitable gapping, as shown in Figure 10, that reduce the fringe of a 1 .8 Tesla (T) sector magnet 302 to less than 10 mT at the cavity 304.
- T 1 .8 Tesla
- Figure 1 1 shows an alternative RF cavity 1 104 including a single RF chamber 1 106 suitable for use with the accelerator stack 130 in accordance with various embodiments. While having only a single RF chamber 1 106, the RF cavity 1 104 is substantially similar to the RF cavity 904 described above in other respects.
- Embodiments of the accelerator stack 130 may include one or more of the RF cavity 304, 904, and/or 1 104 in any combination.
- Some embodiments of the stacked cyclotron 130 may include multiple RF cavities arranged in series between the sector magnets 302.
- Figure 12 shows a pair of sector magnets 1202, 1204 and a pair of RF cavities 1206, 1208 disposed between the sector magnets 1202, 1204.
- the sector magnets 1202 are equivalent to the sector magnet 302 and the RF cavities 1206, 1208 may be any of RF cavities 304, 808, and/or 1 104.
- Outer RF cavity 1208 may be in the outer region where the gap between sector magnets 1202 and 1204 may be greater as they extend radically out from a center of a stacked cyclotron 130.
- Outer RF cavity 1208 may provide additional energy gain per turn. The additional energy gain per turn may provide additional spacing between successive orbits, facilitating low-loss extraction of the beam at its maximum energy.
- FIG. 13 shows a fuel pin based sub-critical core nuclear power generation system 1300 in accordance with various embodiments.
- the fuel pin based sub-critical core nuclear power generation system 1300 includes the accelerator complex 102 described above, a fuel pin based sub-critical core 1302, power generation 1304, and fuel processing complex 1306.
- the core 1302 includes fuel pins 1308 that may include thorium.
- the system 1300 can generate power using thorium-cycle fission. In thorium-cycle fission, thorium ( Th) is transmuted to 233 U for fission.
- Th thorium
- the thorium nucleus is not subject to fission, but it will readily capture a fast neutron, becoming the radioactive isotope 233 Th.
- the 233 Th nucleus decays twice to form the fissionable isotope 233 U.
- the same process of transmutation that creates the 233 U may also transmute fission products generated in the core 1302, limiting the accumulation of long-lived waste isotopes in the core 1302.
- Transmutation of 232 Th and stimulation of 233 U uses fast neutronics.
- the core 1302 uses a large-atomic-weight material (e.g., molten lead, metal, salt, etc.) as moderator.
- the heavy moderator like the heavy carrier salt of the salt 204 described above, allows an energetic (fast) neutron to lose only a small fraction of its energy with each collision or scatter with a moderator nucleus.
- the energy of the neutron decreases slowly as it diffuses and scatters within the core 1302.
- Each neutron thereby retains sufficient energy to have maximum probability to capture on and transmute a 232 Th nucleus, or alternatively to stimulate fission of a 233 U nucleus previously produced through transmutation.
- the accelerator complex 102 generates and injects multiple (e.g., 3 or more) beams of energetic protons into the core 1302 that, via spallation, provide some of the neutrons needed to sustain fission.
- multiple energetic neutrons are released.
- the cumulative energy of the multiple proton beams provides neutrons sufficient for fuel transmutation, and sustaining fission in the sub-critical core 1302.
- the moderator has a relatively large heat capacity and may prevent the core 1302 from heating to a dangerous temperature if the heat transfer systems fail when the core 1302 is shut down.
- a large-atomic-weight material e.g., lead
- Heat from the fission may be transferred via convection through the molten column 1310 (e.g., molten lead) of the core 1302 to heat exchanger 1314 located above core 1302.
- Heat exchanger 1314 transfers the heat from the molten lead to steam which is used to drive steam powered turbine 1316 which, along with generator 1320, generates electricity. As the temperature is increased the thermal efficiency for driving turbine 1316 may improve.
- Pumps 1322, 1324 may facilitate movement of the water and molten lead. In particular, pump 1324 may pump the cooled molten lead back to the bottom of core 1302 to close the heat transfer cycle.
- Condenser 1318 may take the steam that drives turbine 1316 and condense it back into a liquid. Pump 1322 may pump the liquid from condenser 1318 back to heat exchanger 1314 to be converted back into steam.
- FIG 14 illustrates a block diagram of an overhead view of a proton beam distribution pattern in the core 1302 in accordance with various embodiments.
- the thorium fuel of core 1302 is contained in fuel pins 1308 that are assembled into bundles 1450.
- the space between the fuel pins is filled with a molten material, such as lead.
- An additional layer 1460 of molten metal along the outermost radius of core 1302 serves as a neutron reflector.
- core 1302 is driven by seven proton beams 1420 distributed equidistant from one another.
- the distribution of proton beams 1420 may help to maintain the generation of spallation neutrons with a flux that may be approximately homogeneous throughout the region of core 1302 containing thorium fuel.
- beams 1420 may, cumulatively, provide approximately 15 MW of continuous beam power of protons (e.g., corresponding to approximately 12 mA of current at 800 MeV of kinetic energy).
- Each proton beam 1420 is directed from a cyclotron of the cyclotron stack 130 to a different one of spallation zones 1440 within core 1302 through respective evacuated tubes, proton beam injection channels 1430.
- Each proton beam injection channel 1430 may be arranged parallel to the vertical axis of core 1302 (e.g., perpendicular to the top surface of core 1302) and may stop at core 1302 or extend, either fully or partially, through the core 1302.
- Proton beam injection channels 1430 may be disposed in a symmetric pattern within core 1302. This arrangement may have the effect of approximating a volumetric feed of neutrons throughout the core 1302.
- the use of multiple beams 1420 may reduce the attenuation of neutrons in the outer regions of core 1302, allowing the power density of core 1302 to remain relatively flat through a prolonged period of operation.
- the fuel pin bundles 1450 may be used continuously (e.g., without being reshuffled) during the prolonged period of operation.
- Proton beams 1420 injected into each proton beam injection channel 1430, may be scanned by one or more steering elements so that the protons within proton beams 1420 strike the side walls of proton beam injection channels 1430 with an approximately tangential orientation.
- mercury vapor based high-power targeting may be used.
- a mercury vapor target may give optimum targeting for high-power proton or ion beams, yet the target would be a Hg vapor column that is continuously being condensed and re-circulated so that there is nothing that can be destroyed or radiation- damaged.
- a liquid mercury target may be produced as the beam enters a 'fountain' flow of liquid mercury.
- the liquid column may be disrupted by the liquid flow, but recovers shortly thereafter so that a subsequent bunch can be targeted.
- Particular embodiments may comprise a high-density column of mercury vapor.
- the metal mercury has the unique property that it is liquid at room temperature and also has large vapor pressure at moderate temperature.
- a proton strikes the tube wall it passes into the spallation zone 1440 and produces a sequence of nuclear scatterings that yield a longitudinally distributed flux of spallation neutrons around each proton beam 1420.
- a proton having approximately 800MeV of kinetic energy may produce approximately twenty fast neutrons through spallation.
- the spallation neutrons gradually lose energy by elastic collisions with lead nuclei. As the spallation neutrons pass through fuel pins bundles 1450 they can be captured by 232 Th nuclei to transform them into the heavier isotope 233 Th.
- Spallation zone 1440 may comprise a molten metal, such as lead.
- core 1302 may be immersed in a bath of molten metal (e.g., lead).
- the molten metal may fill spallation zones 1440 and serve as a spallation target, a fast neutron moderator, and a medium for convective heat transfer.
- a molten salt slurry may be used instead of molten lead or molten metal.
- molten lead may be chemically active. For example, it may migrate along grain boundaries in steel and other metals. This may lead to corroding of the weak-link attachment between grains so that the metal becomes brittle and subject to fatigue, swelling, and stress cracking.
- a cladding material such as a metal-matrix composite (MMC), in which filaments of ceramic are embedded within a high-strength matrix metal.
- MMC metal-matrix composite
- Certain embodiments may include forming the MMC by coating the ceramic fibers with a nanolayer of titanium. Titanium readily bonds to most ceramics at high temperature, diffusing the titanium into the surface layer of ceramic.
- the titanium surfaced fiber may be coated with a nanolayer of the desired matrix metal.
- the two coatings and the diffusion may be applied under high vacuum, without breaking to air between coatings.
- the titanium may serve as adhesion layer and also to grade tempco.
- the core 1302 may be designed so that it remains safe to restart after an extended down-time.
- core 1302 there may be an inventory of the intermediary isotope 233 Pa.
- 233 Pa may be formed after neutron capture on 232 Th and subsequent rapid beta decay.
- 233 Pa has a one-month half-life for its beta decay into the 233 U that is the fissile fuel.
- the inventory of 233 Pa continues to beta-decay into 233 U over the following months.
- core 1302 is restarted it may have more 233 U than it did when the proton beams were shut-off. This may shift the criticality of the core 1302 by up to 2%.
- Certain embodiments may be designed with that consideration in mind and may thus limit the choice of criticality in designing the core (e.g., it may be designed so that it is impossible for it to go critical under any circumstance.
- the core 1302 may periodically be reloaded with fresh fuel.
- the fresh fuel may include fresh thorium and actinides which are combined in a fuel fabrication block 1328.
- the fresh fuel is loaded into core 1302 while the spent fuel is removed.
- the spent fuel is removed from the core 1302 is sent to a reprocessing block 1326 which removes the fission fragments and sends them to waste packaging 1330 while the actinides are separated and sent to the fuel fabrication 1328 to be combined with the fresh thorium.
- the waste packaging of the fission fragments is then sent to a repository for storage.
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- General Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Particle Accelerators (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US37874110P | 2010-08-31 | 2010-08-31 | |
PCT/US2011/049982 WO2012030970A2 (en) | 2010-08-31 | 2011-08-31 | Accelerator driven sub-critical core |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2612327A2 true EP2612327A2 (en) | 2013-07-10 |
EP2612327A4 EP2612327A4 (en) | 2016-02-24 |
Family
ID=48536637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP11822566.3A Withdrawn EP2612327A4 (en) | 2010-08-31 | 2011-08-31 | Accelerator driven sub-critical core |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP2612327A4 (en) |
KR (1) | KR101515825B1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2557616C1 (en) * | 2014-12-10 | 2015-07-27 | Общество с ограниченной ответственностью "Инжектор" | Method of conversion of nuclear energy into heat energy and device for its implementation (versions) |
RU2624824C1 (en) * | 2016-03-14 | 2017-07-07 | Общество с ограниченной ответственностью "Финансовый партнер" | Method of nuclear energy conversion into thermal and device for its implementation (variants) |
CN109727690B (en) * | 2019-03-18 | 2020-10-09 | 中国原子能科学研究院 | Instrument control system of double-reactor-core zero-power experimental device |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2959980B2 (en) * | 1994-11-24 | 1999-10-06 | 核燃料サイクル開発機構 | Subcritical reactor |
LU90570B1 (en) | 2000-04-26 | 2001-10-29 | Europ Economic Community | Method of incineration of minor actinides in nuclear reactors |
JP2005024457A (en) | 2003-07-04 | 2005-01-27 | Mitsubishi Heavy Ind Ltd | Accelerator driven nucleus transformation system, irradiation system, and flow guide |
-
2011
- 2011-08-31 KR KR1020137008168A patent/KR101515825B1/en active IP Right Grant
- 2011-08-31 EP EP11822566.3A patent/EP2612327A4/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
KR20130079521A (en) | 2013-07-10 |
KR101515825B1 (en) | 2015-05-04 |
EP2612327A4 (en) | 2016-02-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8983017B2 (en) | Accelerator driven sub-critical core | |
EP0725967B2 (en) | An energy amplifier for "clean" nuclear energy production driven by a particle beam accelerator | |
Bagryansky et al. | Gas dynamic trap as high power 14 MeV neutron source | |
Rubbia et al. | A tentative programme towards a full scale energy amplifier | |
Stacey et al. | Resolution of fission and fusion technology integration issues: an upgraded design concept for the subcritical advanced burner reactor | |
Moir et al. | Mirror-based hybrids of recent design | |
Moir et al. | Axisymmetric magnetic mirror fusion-fission hybrid | |
KR101515825B1 (en) | Accelerator driven sub-critical core | |
WO2012030970A2 (en) | Accelerator driven sub-critical core | |
Logan | The Mirror Advanced Reactor Study (MARS) | |
Fernandez et al. | A preliminary estimate of the economic impact of the energy amplifier | |
Fietier et al. | A cyclotron-based accelerator for driving the energy amplifier | |
Rimpault et al. | General Synthesis Report of the Different ADS Design Status. Establishment of a Catalogue of the R&D needs | |
Abdou et al. | Fusion Reactor Design IV (Report on the 4th IAEA Technical Committee Meeting and Workshop, Yalta, USSR, 26 May–6 June 1986) | |
Moir et al. | Fusion–Fission Hybrid Reactors | |
Ågren et al. | The hybrid reactor project based on the straight field line mirror concept | |
Thomassen et al. | A technology demonstration facility | |
Bermejo et al. | Neutron sources | |
Nelson et al. | Engineering overview of the Minimars reactor | |
Emmert | TASKA-M—a low cost technology test tandem mirror | |
Takahashi | Brookhaven National Laboratory ADS concepts (USA) | |
DeBellis et al. | Fusion power: status and options | |
Conn et al. | Studies of the physics and engineering of deuterium-deuterium barrier tandem mirror reactors | |
Steinberg et al. | Spallator: a new option for nuclear power | |
Ågren et al. | Conceptual study of a straight field line mirror hybrid reactor |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20130328 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20160125 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: G21C 11/06 20060101ALN20160119BHEP Ipc: G21C 11/08 20060101ALN20160119BHEP Ipc: G21G 1/02 20060101ALI20160119BHEP Ipc: H05H 13/00 20060101AFI20160119BHEP Ipc: G21C 3/54 20060101ALN20160119BHEP Ipc: G21C 1/30 20060101ALI20160119BHEP |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20160823 |