US20200075182A1 - Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof - Google Patents
Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof Download PDFInfo
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- US20200075182A1 US20200075182A1 US16/394,322 US201916394322A US2020075182A1 US 20200075182 A1 US20200075182 A1 US 20200075182A1 US 201916394322 A US201916394322 A US 201916394322A US 2020075182 A1 US2020075182 A1 US 2020075182A1
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- Prior art keywords
- slug
- metallic
- nuclear fuel
- metallic fuel
- fuel slug
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- 239000000446 fuel Substances 0.000 title claims abstract description 274
- 239000003758 nuclear fuel Substances 0.000 title claims abstract description 182
- 239000010410 layer Substances 0.000 title claims abstract description 167
- 239000011253 protective coating Substances 0.000 title claims abstract description 44
- 238000004519 manufacturing process Methods 0.000 title abstract description 57
- 238000000034 method Methods 0.000 title abstract description 47
- 238000005253 cladding Methods 0.000 claims abstract description 105
- 230000004992 fission Effects 0.000 claims abstract description 10
- 150000004767 nitrides Chemical class 0.000 claims description 33
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 24
- 238000007789 sealing Methods 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 8
- 239000011651 chromium Substances 0.000 claims description 7
- 239000010955 niobium Substances 0.000 claims description 7
- 239000010936 titanium Substances 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- 229910052770 Uranium Inorganic materials 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 239000011572 manganese Substances 0.000 claims description 4
- 229910052758 niobium Inorganic materials 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 3
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 229910052715 tantalum Inorganic materials 0.000 claims description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 59
- 239000011248 coating agent Substances 0.000 abstract description 7
- 238000000576 coating method Methods 0.000 abstract description 7
- 239000012535 impurity Substances 0.000 abstract description 7
- 230000000087 stabilizing effect Effects 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- 239000007789 gas Substances 0.000 description 28
- 230000003647 oxidation Effects 0.000 description 21
- 238000007254 oxidation reaction Methods 0.000 description 21
- 238000002474 experimental method Methods 0.000 description 17
- 238000010438 heat treatment Methods 0.000 description 17
- 238000009792 diffusion process Methods 0.000 description 16
- 239000000843 powder Substances 0.000 description 16
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 10
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 10
- 238000001000 micrograph Methods 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000007598 dipping method Methods 0.000 description 9
- 230000003993 interaction Effects 0.000 description 9
- 230000008569 process Effects 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 238000007743 anodising Methods 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 description 5
- 239000001569 carbon dioxide Substances 0.000 description 5
- 229910002091 carbon monoxide Inorganic materials 0.000 description 5
- 239000011247 coating layer Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 238000007745 plasma electrolytic oxidation reaction Methods 0.000 description 4
- 230000009466 transformation Effects 0.000 description 4
- 229910052726 zirconium Inorganic materials 0.000 description 4
- 229910052778 Plutonium Inorganic materials 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910052776 Thorium Inorganic materials 0.000 description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000005121 nitriding Methods 0.000 description 3
- 229910052761 rare earth metal Inorganic materials 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 2
- 229910052695 Americium Inorganic materials 0.000 description 2
- 229910052684 Cerium Inorganic materials 0.000 description 2
- 229910052685 Curium Inorganic materials 0.000 description 2
- 229910052693 Europium Inorganic materials 0.000 description 2
- 229910052688 Gadolinium Inorganic materials 0.000 description 2
- 241000237858 Gastropoda Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910052779 Neodymium Inorganic materials 0.000 description 2
- 229910052781 Neptunium Inorganic materials 0.000 description 2
- 229910052772 Samarium Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910052768 actinide Inorganic materials 0.000 description 2
- 150000001255 actinides Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000010891 electric arc Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 229910052746 lanthanum Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- -1 oxide Chemical class 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- OYEHPCDNVJXUIW-UHFFFAOYSA-N plutonium atom Chemical compound [Pu] OYEHPCDNVJXUIW-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- 229910052773 Promethium Inorganic materials 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- LXQXZNRPTYVCNG-UHFFFAOYSA-N americium atom Chemical compound [Am] LXQXZNRPTYVCNG-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 239000008204 material by function Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
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- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- LFNLGNPSGWYGGD-UHFFFAOYSA-N neptunium atom Chemical compound [Np] LFNLGNPSGWYGGD-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- VQMWBBYLQSCNPO-UHFFFAOYSA-N promethium atom Chemical compound [Pm] VQMWBBYLQSCNPO-UHFFFAOYSA-N 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005245 sintering Methods 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
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Images
Classifications
-
- 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
- G21C3/02—Fuel elements
- G21C3/04—Constructional details
- G21C3/16—Details of the construction within the casing
- G21C3/20—Details of the construction within the casing with coating on fuel or on inside of casing; with non-active interlayer between casing and active material with multiple casings or multiple active layers
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C1/00—Reactor types
- G21C1/02—Fast fission reactors, i.e. reactors not using a moderator ; Metal cooled reactors; Fast breeders
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C21/00—Apparatus or processes specially adapted to the manufacture of reactors or parts thereof
- G21C21/02—Manufacture of fuel elements or breeder elements contained in non-active casings
-
- 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
- G21C3/58—Solid reactor fuel Pellets made of fissile material
- G21C3/60—Metallic fuel; Intermetallic dispersions
-
- 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
- G21C3/02—Fuel elements
- G21C3/04—Constructional details
-
- 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
- G21C3/02—Fuel elements
- G21C3/04—Constructional details
- G21C3/045—Pellets
- G21C3/047—Pellet-clad interaction
-
- 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 relates to a nuclear fuel rod for fast reactors that includes a metallic fuel slug coated with a protective coating layer and a fabrication method thereof.
- the present invention relates to a process for improving the performance of nuclear fuel for reactors, and more particularly, to a technique that stabilizes components of a metallic fuel slug and fission products or impurities through the stabilization of surfaces of the metallic fuel slug and metallic fuel powder by a surface treatment.
- Nuclear fuel in fast reactors is designed in various types, such as a plate type, a pellet type, and a rod type, and a fissionable material that undergoes a nuclear reaction is included in a nuclear fuel rod.
- the fissionable material is sealed by a container, which is not reactive due to its good compatibility with a coolant and has good heat transfer characteristics, i.e. a cladding tube.
- the nuclear fuel rods being maintained at a constant spacing are assembled in the form of a fuel assembly and the assembly is charged into a nuclear reactor.
- the cladding tube surrounding the fuel must prevent chemical interactions between the fissionable material and the coolant by blocking a direct contact therebetween and must prevent the leakage of fission products.
- a phenomenon occurs, in which a melting temperature of a metallic fuel slug decreases or the strength of a cladding tube decreases by the interpenetration between components (uranium (U), plutonium (Pu), thorium (Th), minor actinides (MA), zirconium (Zr), molybdenum (Mo), fission products, etc.) of the metallic fuel slug and components (iron (Fe), chromium (Cr), tungsten (W), Mo, vanadium (V), niobium (Nb), etc.) of the stainless steel cladding tube by diffusion.
- components uranium (U), plutonium (Pu), thorium (Th), minor actinides (MA), zirconium (Zr), molybdenum (Mo), fission products, etc.
- the maximum allowable bumup and the maximum allowable operating temperature of the metallic fuel for fast reactors may be limited [J. Nucl. Mater., 204 (1993) p. 244-251 and J. Nucl. Mater., 204 (1993) p. 141-147].
- GE General Electric
- GE disclosed a technique for inhibiting the interaction between a metallic fuel slug and a cladding tube by inserting an about 50 ⁇ m thick liner or sleeve formed of a metal of Zr, titanium (Ti), Nb, and Mo between the metallic fuel slug and the cladding tube.
- Metallic fuel for reactors has been considered important as a nuclear fuel of sodium-cooled fast reactors, an advanced nuclear fuel, due to high thermal conductivity and high nuclear proliferation resistance in conjunction with pyroprocessing.
- metallic fuel since metallic uranium as a fuel material and a fuel cladding material interdiffuse and react above 650° C., i.e., an operating temperature of the reactor, the thickness of a cladding tube decreases according to the operating time. As a result, the lifetime of the cladding tube may decrease due to the deterioration of the soundness thereof.
- research into using a material for preventing the interdiffusion and reaction between the fuel and the cladding tube has been conducted.
- Patent Document 1 Korean Patent Application Laid-Open Publication No. KR-2009-0018396
- a nuclear fuel rod for fast reactors in which an oxide coating layer is formed on the inside of a cladding tube, is suggested in order to inhibit the fuel-cladding material interaction.
- a concept of attaching chromium oxide, vanadium oxide, and zirconium oxide to the inside of the cladding tube by using an acid dissolution and oxidation method, a high-temperature oxidation method, an electrolytic oxidation method, and a vapor deposition method is suggested.
- Patent Document 2 Korean Patent Application Laid-Open Publication No. KR-2010-0114392
- a concept of depositing functional materials, such as titanium, nickel, chromium, vanadium, and zirconium, in multilayers is suggested in order to inhibit the fuel-cladding material interaction and improve the performance of the fuel cladding tube.
- Patent Document 3 Korean Patent Application Laid-Open Publication No. KR-2010-0081961
- a method of uniformly plating an inner wall of a fuel cladding tube and a concept of forming a nitride layer on a surface of the plating layer through an additional process of a nitridation treatment are suggested.
- Patent Document 4 Japanese Patent Application Laid-Open Publication No. 2012-237574
- a typical main body that may accommodate nuclear fuel and is formed of an iron-based material
- a cladding tube including an inner layer part composed of a carbon-based material that is formed on an inner circumferential surface of the main body and a reactor including the cladding tube are suggested in order to provide a cladding tube that may improve high-temperature characteristics and power generation efficiency, and a reactor including the cladding tube.
- the fuel cladding tube for fast reactors is a seamless tube having a diameter of 7 mm, a thickness of 0.6 mm, and a length of 3,000 mm.
- the functional material for preventing interdiffusion to the inside of the thin and long tube may be high.
- the present inventors found that the interdiffusion between a metallic fuel slug and a cladding tube may be prevented by stabilizing components of the metallic fuel slug and fission products or impurities though the simple and uniform formation of an oxide layer, a nitride layer, or a carbide layer on the surface of the metallic fuel slug, thereby leading to completion of the present invention.
- One object of the present invention is to provide a metallic fuel slug coated with a protective coating layer.
- Another object of the present invention is to provide a nuclear fuel rod for fast reactors including the metallic fuel slug.
- Still another object of the present invention is to provide a method of fabricating the nuclear fuel rod for fast reactors.
- the present invention provides a metallic fuel slug used in a nuclear fuel rod for fast reactors, the metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug.
- the present invention also provides a nuclear fuel rod for fast reactors including: a metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug; and a cladding tube sealing the metal fuel slug.
- the present invention provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of a metallic fuel slug with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel slug (step 1); and sealing a cladding tube after introducing the metallic fuel slug coated with the protective coating layer in step 1 into the cladding tube (step 2).
- the present invention also provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of metallic fuel powder with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel powder (step 1); preparing a metallic fuel slug by forming the metallic fuel powder coated with the protective coating layer in step 1 (step 2); and sealing a cladding tube after introducing the metallic fuel slug prepared in step 2 into the cladding tube (step 3).
- a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel powder
- FIG. 1 is a schematic view illustrating a metallic fuel slug coated with a protective coating layer according to the present invention
- FIG. 2 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 1 of the present invention after a diffusion couple experiment;
- FIG. 3 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 2 of the present invention after a diffusion couple experiment;
- FIG. 4 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 3 of the present invention after a diffusion couple experiment;
- FIG. 5 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 18 of the present invention after a diffusion couple experiment;
- FIG. 6 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Comparative Example 1 of the present invention after a diffusion couple experiment.
- the present invention provides a metallic fuel slug used in a nuclear fuel rod for fast reactors, the metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug.
- the performance of the metallic fuel may be improved.
- the metallic fuel slug may be fabricated by including uranium (U), plutonium (Pu), thorium (Th), minor actinides (MA, neptunium (Np), americium (Am), and curium (Cm)), rare earth elements (RE, lanthanum (La), cerium (Ce), neodymium (Nd), praseodymium (Pr), promethium (Pm), samarium (Sm), europium (Eu), and gadolinium (Gd)), zirconium (Zr), and molybdenum (Mo) alone or in a mixture thereof.
- any metallic fuel slug applicable to the nuclear fuel rod for fast reactors may be used.
- a thickness of the protective coating layer may be in a range of 0.5 ⁇ m to 100 ⁇ m.
- the thickness of the protective coating layer is less than 0.5 ⁇ m, the interdiffusion phenomenon may not be sufficiently inhibited.
- the thickness of the protective coating layer is greater than 100 ⁇ m, since thermal conductivity may decrease due to the thick coating layer, heat discharged from the fuel may not be efficiently transferred.
- the present invention also provides a nuclear fuel rod for fast reactors including a metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug; and a cladding tube sealing the metal fuel slug.
- the metallic fuel slug may be fabricated by including U, Pu, Th, MA (Np, Am, and Cm), RE (La, Ce, Nd, Pr, Pm, Sm, Eu, and Gd), Zr, and Mo alone or in a mixture thereof.
- MA Np, Am, and Cm
- RE La, Ce, Nd, Pr, Pm, Sm, Eu, and Gd
- Zr Zr
- Mo Mo alone or in a mixture thereof.
- any metallic fuel slug applicable to the nuclear fuel rod for fast reactors may be used.
- a thickness of the protective coating layer may be in a range of 0.5 ⁇ m to 100 ⁇ m.
- the thickness of the protective coating layer is less than 0.5 ⁇ m, the interdiffusion phenomenon may not be sufficiently inhibited.
- the thickness of the protective coating layer is greater than 100 ⁇ m, since thermal conductivity may decrease due to the thick coating layer, heat discharged from the fuel may not be efficiently transferred.
- the cladding tube may include iron (Fe), chromium (Cr), tungsten (W), Mo, vanadium (V), titanium (Ti), niobium (Nb), tantalum (Ta), silicon (Si), manganese (Mn), nickel (Ni), carbon (C), nitrogen (N), and boron (B) alone or in the form of an alloy by mixing thereof.
- the present invention is not limited thereto.
- the present invention provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of a metallic fuel slug with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel slug (step 1); and sealing a cladding tube after introducing the metallic fuel slug coated with the protective coating layer in step 1 into the cladding tube (step 2).
- step 1 is a step of forming the protective coating layer on the surface of the metallic fuel slug.
- an oxide, nitride, or carbide coating layer may be formed on the surface of the metallic fuel slug by oxidation, nitridation, or caburization of the metallic fuel slug.
- step 2 is a step of sealing the cladding tube after introducing the surface-treated metallic fuel slug into the cladding tube.
- a method of heat treating in a gas atmosphere containing oxygen, a method of dipping in an oxidation solution, and a method of performing an electrolytic treatment may be used as a method of forming an oxide protective coating layer.
- the method of heat treating in a gas atmosphere containing oxygen may be performed by heat treating a metallic fuel slug at a temperature ranging from 100° C. to 1000° C. and a pressure ranging from 1 atm to 50 atm in an atmosphere of oxygen, air, or inert gas containing oxygen.
- the oxide layer may not be efficiently formed.
- the heat treatment temperature is greater than 1000° C.
- transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded.
- a pressurization treatment may be performed for the efficient heat treatment.
- the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- the method of dipping in an oxidation solution may be performed by dipping a metallic fuel slug in a hydrochloric, sulfuric, nitric, sodium hydroxide, or potassium hydroxide solution, and heat treating the metallic fuel slug at a temperature ranging from 30° C. to 90° C. for 30 minutes to 5 hours.
- the method of performing an electrolytic treatment may be performed by plasma electrolytic oxidation, micro-arc oxidation, micro-arc discharge oxidation, spark anodizing, anodic spark deposition, micro-arc anodizing, micro plasma anodizing, micro plasma oxidation, and electro plasma oxidation of a metallic fuel slug.
- a method of heat treating in a gas atmosphere containing nitrogen and an ion nitriding method may be used as a method of forming a nitride protective coating layer.
- the method of heat treating in a gas atmosphere containing nitrogen may be performed by heat treating a metallic fuel slug at a temperature ranging from 100° C. to 1000° C. and a pressure ranging from 1 atm to 50 atm in an atmosphere of nitrogen, ammonia, or inert gas containing nitrogen.
- the heat treatment temperature is less than 100° C.
- the nitride layer may not be efficiently formed.
- the heat treatment temperature is greater than 1000° C.
- transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded.
- a pressurization treatment may be performed for the efficient heat treatment.
- the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- the ion nitriding method may be performed by using a method of applying a negative potential to an object to be ion-nitrided in a gas atmosphere containing nitrogen.
- the ion nitriding method may be completed by heat treating the object under conditions of a temperature ranging from 100° C. to 1000° C., a pressure ranging from 1 atm to 50 atm, and a potential ranging from 1 V to 1,000 V in an inert atmosphere containing nitrogen. In the case that the heat treatment temperature is less than 100° C., the nitride layer may not be efficiently formed.
- the heat treatment temperature is greater than 1000° C.
- transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded.
- a pressurization treatment may be performed for the efficient heat treatment.
- the pressure of the heat treatment is 50 atm or more
- an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- efficient ion nitridation may not be achieved at a potential of less than 1 V. Since an additional insulation treatment may be required at a potential of greater than 1,000 V, economic efficiency of the process may be reduced.
- a method of heat treating in a gas atmosphere containing carbon may be used as a method of forming a carbide protective coating layer.
- the method of heat treating in a gas atmosphere containing carbon may be performed by heat treating a metallic fuel slug at a temperature ranging from 100° C. to 1000° C. and a pressure ranging from 1 atm to 50 atm in an atmosphere of carbon, methane, carbon dioxide, or carbon monoxide.
- the carbide layer may not be efficiently formed.
- the heat treatment temperature is greater than 1000° C.
- transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded.
- a pressurization treatment may be performed for the efficient heat treatment.
- the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- the present invention provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of metallic fuel powder with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel powder (step 1); preparing a metallic fuel slug by forming the metallic fuel powder coated with the protective coating layer in step 1 (step 2); and sealing a cladding tube after introducing the metallic fuel slug prepared in step 2 into the cladding tube (step 3).
- the method of fabricating a nuclear fuel rod for fast reactors may form the protective coating layer on the surface of the metallic fuel powder, components of fuel, fission products, or impurities may be stabilized and various types of fuels may be fabricated.
- the coated metallic fuel powder may be formed in the form of a metallic fuel slug during the fabrication of the nuclear fuel rod for fast reactors and thus, the interdiffusion phenomenon between the metallic fuel slug and the cladding tube sealing the metallic fuel slug may be reduced.
- step 1 is a step of forming the protective coating layer on the surface of the metallic fuel powder.
- an oxide, nitride, or carbide coating layer may be formed on the surface of the metallic fuel powder by oxidation, nitridation, or caburization of the metallic fuel powder.
- Preferred conditions that may form the protective layers are as described in the above specification.
- step 2 is a step of preparing the metallic fuel slug by forming the metallic fuel powder. Specifically, a method of stacking the powder in a nuclear fuel rod composed of a cylindrical cladding tube, a method of sintering the powder by heat treating in a heat treatment furnace, and a method of forming a cylindrical sintered body by introducing the metallic fuel powder into a metal or ceramic matrix and heat treating.
- step 3 is a step of sealing the cladding tube after introducing the metallic fuel slug into the cladding tube.
- the nuclear fuel rod for fast reactors that includes the surface treated metallic fuel slug and the cladding tube according to the present invention has an excellent effect of stabilizing components of the metallic fuel slug and fission products or impurities, because the interdiffusion between the metallic fuel slug and the cladding tube does not occur. Also, since the uniform coating on the surface of the metallic fuel slug may be facilitated and fabrication costs may be significantly reduced in comparison to a typical technique of using a functional material for preventing the interdiffusion at an inner surface of the cladding tube, it may be suitable for fabricating the nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 600° C. and a pressure of 5 atm for 2 hours in an argon gas atmosphere containing 20% oxygen. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 1 hour in an air atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 1 hour in an air atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a hydrochloric acid solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a sulfuric acid solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a nitric acid solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a sodium hydroxide solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a potassium hydroxide solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug through plasma electrolytic oxidation by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a potassium hydroxide solution and a sodium hydroxide solution, and then applying a positive voltage of 200 V thereto. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro-arc oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro-arc discharge oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by spark anodizing of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by anodic spark deposition of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro-arc anodizing of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro plasma anodizing of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro plasma oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by electro plasma oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 800° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 800° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 500° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 300° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 150° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 700° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 500° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 300° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 150° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 700° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 700° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 700° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- a surface treatment was not performed on a metallic fuel slug formed of U-10Zr, a nuclear fuel material, and the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- the nuclear fuel rods for fast reactors fabricated in Examples 1, 2, 3, and 18, and Comparative Example 1 were cut to a length of 10 mm, and the 10 mm long nuclear fuel rods were then cut in half in a radial direction. Then, metallic fuel slug-cladding tube diffusion couple experiments were performed at 800° C. for 25 hours. After the diffusion couple experiments, bonded samples were cooled and cross sections of the bonded samples were observed using a scanning electron microscope. The results thereof are presented in FIGS. 2 to 6 .
- FIG. 2 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 1 of the present invention after the diffusion couple experiment.
- FIG. 3 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 2 of the present invention after the diffusion couple experiment.
- FIG. 4 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 3 of the present invention after the diffusion couple experiment.
- FIG. 5 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 18 of the present invention after the diffusion couple experiment.
- FIG. 6 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Comparative Example 1 of the present invention after the diffusion couple experiment.
- Example 1 As illustrated in FIGS. 2 to 6 , with respect to Example 1 ( FIG. 2 ), Example 2 ( FIG. 3 ), Example 3 ( FIG. 4 ), and Example 18 ( FIG. 5 ), it was observed that the interactions between the metallic fuel slugs and the cladding tubes did not occur because dense oxide layers and nitride layer were formed on the surfaces of the metallic fuel slugs. In contrast, with respect to Comparative Example 1 ( FIG. 6 ), it may be observed that the metallic fuel slug material and the cladding tube material were interdiffused and reacted during the diffusion couple experiment.
- the nuclear fuel rod for fast reactors that includes the surface treated metallic fuel slug and the cladding tube according to the present invention had an excellent effect of stabilizing components of the metallic fuel slug and fission products or impurities, because the interdiffusion between the metallic fuel slug and the cladding tube did not occur. Also, since the uniform coating on the surface of the metallic fuel slug may be facilitated and fabrication costs may be significantly reduced in comparison to a typical technique of using a functional material for preventing the interdiffusion at an inner surface of the cladding tube, it may be suitable for fabricating the nuclear fuel rod for fast reactors.
- a rare earth element which is included on the surface of a metallic fuel fabricated by pyroprocessing to degrade the performance of the metallic fuel, may be transformed into a non-active compound, such as oxide, nitride, and carbide, the improvement of the performance of the metallic fuel and the extension of the lifetime of the metallic fuel may be expected.
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Abstract
Description
- This patent application is a divisional application of U.S. application Ser. No. 15/412,560, filed on Jan. 23, 2017, which is a continuation application of U.S. application Ser. No. 14/079,740, filed on Nov. 14, 2013, now U.S. Pat. No. 9,589,680, issued Mar. 7, 2017, which claims the benefit of priority from Korean Patent Application No. 10-2013-0005989 filed on Jan. 18, 2013, and Korean Patent Application No. 10-2013-0110624 filed on Sep. 13, 2013, the contents of which are incorporated herein by reference.
- The present disclosure relates to a nuclear fuel rod for fast reactors that includes a metallic fuel slug coated with a protective coating layer and a fabrication method thereof.
- The present invention relates to a process for improving the performance of nuclear fuel for reactors, and more particularly, to a technique that stabilizes components of a metallic fuel slug and fission products or impurities through the stabilization of surfaces of the metallic fuel slug and metallic fuel powder by a surface treatment.
- Nuclear fuel in fast reactors is designed in various types, such as a plate type, a pellet type, and a rod type, and a fissionable material that undergoes a nuclear reaction is included in a nuclear fuel rod. The fissionable material is sealed by a container, which is not reactive due to its good compatibility with a coolant and has good heat transfer characteristics, i.e. a cladding tube. The nuclear fuel rods being maintained at a constant spacing are assembled in the form of a fuel assembly and the assembly is charged into a nuclear reactor. In this case, the cladding tube surrounding the fuel must prevent chemical interactions between the fissionable material and the coolant by blocking a direct contact therebetween and must prevent the leakage of fission products. In addition, in fast reactors using metallic nuclear fuel, it is highly advantageous in terms of the safety and economic efficiency of nuclear fuel to also inhibit interactions between the cladding tube and the fissionable material.
- In particular, in fast reactors using metallic fuel, a phenomenon occurs, in which a melting temperature of a metallic fuel slug decreases or the strength of a cladding tube decreases by the interpenetration between components (uranium (U), plutonium (Pu), thorium (Th), minor actinides (MA), zirconium (Zr), molybdenum (Mo), fission products, etc.) of the metallic fuel slug and components (iron (Fe), chromium (Cr), tungsten (W), Mo, vanadium (V), niobium (Nb), etc.) of the stainless steel cladding tube by diffusion. Thus, the maximum allowable bumup and the maximum allowable operating temperature of the metallic fuel for fast reactors may be limited [J. Nucl. Mater., 204 (1993) p. 244-251 and J. Nucl. Mater., 204 (1993) p. 141-147].
- Also, a diffusion couple experiment performed at 923 K by T. Ogata et al. demonstrated the occurrence of a reaction due to the interdiffusion between a metallic fuel slug and a cladding tube, and reported that the thickness of an interaction layer increased proportional to the reaction time [J. Nucl. Mater., 250 (1997) p. 171-175].
- In order to prevent the interdiffusion reaction, General Electric (GE) disclosed a technique for inhibiting the interaction between a metallic fuel slug and a cladding tube by inserting an about 50 μm thick liner or sleeve formed of a metal of Zr, titanium (Ti), Nb, and Mo between the metallic fuel slug and the cladding tube.
- Since the technique of GE essentially requires the introduction of an additional process, the production of the nuclear fuel rod may not only be complicated, but considerable additional costs may also be required.
- Also, in order to remove quartz tube mold waste generated during the preparation of a fuel slug for fast reactors and simultaneously, to inhibit a fuel-cladding chemical interaction (FCCI) between metallic fuel slug and cladding tube, D. C. Crawford et al. melt-casted an about 200 μm thick zirconium tube and reported the results of their experiments. However, cracks may occur in the zirconium tube.
- Metallic fuel for reactors has been considered important as a nuclear fuel of sodium-cooled fast reactors, an advanced nuclear fuel, due to high thermal conductivity and high nuclear proliferation resistance in conjunction with pyroprocessing. However, with respect to the metallic fuel, since metallic uranium as a fuel material and a fuel cladding material interdiffuse and react above 650° C., i.e., an operating temperature of the reactor, the thickness of a cladding tube decreases according to the operating time. As a result, the lifetime of the cladding tube may decrease due to the deterioration of the soundness thereof. In order to prevent the interaction phenomenon and improve the performance of the cladding material, research into using a material for preventing the interdiffusion and reaction between the fuel and the cladding tube has been conducted.
- In Patent Document 1 (Korean Patent Application Laid-Open Publication No. KR-2009-0018396), a nuclear fuel rod for fast reactors, in which an oxide coating layer is formed on the inside of a cladding tube, is suggested in order to inhibit the fuel-cladding material interaction. Specifically, a concept of attaching chromium oxide, vanadium oxide, and zirconium oxide to the inside of the cladding tube by using an acid dissolution and oxidation method, a high-temperature oxidation method, an electrolytic oxidation method, and a vapor deposition method is suggested.
- In Patent Document 2 (Korean Patent Application Laid-Open Publication No. KR-2010-0114392), a concept of depositing functional materials, such as titanium, nickel, chromium, vanadium, and zirconium, in multilayers is suggested in order to inhibit the fuel-cladding material interaction and improve the performance of the fuel cladding tube.
- In Patent Document 3 (Korean Patent Application Laid-Open Publication No. KR-2010-0081961), a method of uniformly plating an inner wall of a fuel cladding tube and a concept of forming a nitride layer on a surface of the plating layer through an additional process of a nitridation treatment are suggested.
- In Patent Document 4 (Japanese Patent Application Laid-Open Publication No. 2012-237574), a typical main body that may accommodate nuclear fuel and is formed of an iron-based material; and a cladding tube including an inner layer part composed of a carbon-based material that is formed on an inner circumferential surface of the main body and a reactor including the cladding tube are suggested in order to provide a cladding tube that may improve high-temperature characteristics and power generation efficiency, and a reactor including the cladding tube.
- However, the fuel cladding tube for fast reactors is a seamless tube having a diameter of 7 mm, a thickness of 0.6 mm, and a length of 3,000 mm. Thus, there may be limitations in attaching the functional material for preventing interdiffusion to the inside of the thin and long tube, and treatment costs may be high.
- Accordingly, the present inventors found that the interdiffusion between a metallic fuel slug and a cladding tube may be prevented by stabilizing components of the metallic fuel slug and fission products or impurities though the simple and uniform formation of an oxide layer, a nitride layer, or a carbide layer on the surface of the metallic fuel slug, thereby leading to completion of the present invention.
- One object of the present invention is to provide a metallic fuel slug coated with a protective coating layer.
- Another object of the present invention is to provide a nuclear fuel rod for fast reactors including the metallic fuel slug.
- Still another object of the present invention is to provide a method of fabricating the nuclear fuel rod for fast reactors.
- In order to achieve the object, the present invention provides a metallic fuel slug used in a nuclear fuel rod for fast reactors, the metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug.
- The present invention also provides a nuclear fuel rod for fast reactors including: a metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug; and a cladding tube sealing the metal fuel slug.
- Furthermore, the present invention provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of a metallic fuel slug with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel slug (step 1); and sealing a cladding tube after introducing the metallic fuel slug coated with the protective coating layer in
step 1 into the cladding tube (step 2). - The present invention also provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of metallic fuel powder with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel powder (step 1); preparing a metallic fuel slug by forming the metallic fuel powder coated with the protective coating layer in step 1 (step 2); and sealing a cladding tube after introducing the metallic fuel slug prepared in
step 2 into the cladding tube (step 3). - The above and other objects, features and other advantages of the present invention will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
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FIG. 1 is a schematic view illustrating a metallic fuel slug coated with a protective coating layer according to the present invention; -
FIG. 2 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 1 of the present invention after a diffusion couple experiment; -
FIG. 3 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 2 of the present invention after a diffusion couple experiment; -
FIG. 4 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 3 of the present invention after a diffusion couple experiment; -
FIG. 5 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Example 18 of the present invention after a diffusion couple experiment; and -
FIG. 6 is a scanning electron microscope image of a cross section of a nuclear fuel rod for fast reactors according to Comparative Example 1 of the present invention after a diffusion couple experiment. - Features and advantages of the present invention will be more clearly understood by the following detailed description of the present preferred embodiments by reference to the accompanying drawings. It is first noted that terms or words used herein should be construed as meanings or concepts corresponding with the technical sprit of the present invention, based on the principle that the inventor can appropriately define the concepts of the terms to best describe his own invention. Also, it should be understood that detailed descriptions of well-known functions and structures related to the present invention will be omitted so as not to unnecessarily obscure the important point of the present invention.
- Hereinafter, the present invention will be described in detail.
- The present invention provides a metallic fuel slug used in a nuclear fuel rod for fast reactors, the metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug.
- In the metallic fuel slug coated with a protective coating layer according to the present invention, since components of the metallic fuel slug, fission products, or impurities are stabilized, an interdiffusion phenomenon occurred between the metallic fuel slug and the cladding tube sealing the metallic fuel slug during the fabrication of the nuclear fuel rod for fast reactors may be reduced. Also, according to the present invention, since a rare earth element, which is included on the surface of a metallic fuel fabricated by pyroprocessing to degrade the performance of the metallic fuel, may be transformed into a non-active compound, such as oxide, nitride, and carbide, the performance of the metallic fuel may be improved.
- With respect to the metallic fuel slug according to the present invention, the metallic fuel slug may be fabricated by including uranium (U), plutonium (Pu), thorium (Th), minor actinides (MA, neptunium (Np), americium (Am), and curium (Cm)), rare earth elements (RE, lanthanum (La), cerium (Ce), neodymium (Nd), praseodymium (Pr), promethium (Pm), samarium (Sm), europium (Eu), and gadolinium (Gd)), zirconium (Zr), and molybdenum (Mo) alone or in a mixture thereof. However, any metallic fuel slug applicable to the nuclear fuel rod for fast reactors may be used.
- With respect to the metallic fuel slug according to the present invention, a thickness of the protective coating layer may be in a range of 0.5 μm to 100 μm.
- In the case that the thickness of the protective coating layer is less than 0.5 μm, the interdiffusion phenomenon may not be sufficiently inhibited. In the case in which the thickness of the protective coating layer is greater than 100 μm, since thermal conductivity may decrease due to the thick coating layer, heat discharged from the fuel may not be efficiently transferred.
- The present invention also provides a nuclear fuel rod for fast reactors including a metallic fuel slug having a surface coated with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer, wherein the protective coating layer is formed by oxidation, nitridation, or caburization of the metallic fuel slug; and a cladding tube sealing the metal fuel slug.
- With respect to the nuclear fuel rod for fast reactors according to the present invention, the metallic fuel slug may be fabricated by including U, Pu, Th, MA (Np, Am, and Cm), RE (La, Ce, Nd, Pr, Pm, Sm, Eu, and Gd), Zr, and Mo alone or in a mixture thereof. However, any metallic fuel slug applicable to the nuclear fuel rod for fast reactors may be used.
- With respect to the nuclear fuel rod for fast reactors according to the present invention, a thickness of the protective coating layer may be in a range of 0.5 μm to 100 μm.
- In the case that the thickness of the protective coating layer is less than 0.5 μm, the interdiffusion phenomenon may not be sufficiently inhibited. In the case in which the thickness of the protective coating layer is greater than 100 μm, since thermal conductivity may decrease due to the thick coating layer, heat discharged from the fuel may not be efficiently transferred.
- With respect to the nuclear fuel rod for fast reactors according to the present invention, the cladding tube may include iron (Fe), chromium (Cr), tungsten (W), Mo, vanadium (V), titanium (Ti), niobium (Nb), tantalum (Ta), silicon (Si), manganese (Mn), nickel (Ni), carbon (C), nitrogen (N), and boron (B) alone or in the form of an alloy by mixing thereof. However, the present invention is not limited thereto.
- Furthermore, the present invention provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of a metallic fuel slug with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel slug (step 1); and sealing a cladding tube after introducing the metallic fuel slug coated with the protective coating layer in
step 1 into the cladding tube (step 2). - In the fabricating method according to the present invention,
step 1 is a step of forming the protective coating layer on the surface of the metallic fuel slug. Specifically, an oxide, nitride, or carbide coating layer may be formed on the surface of the metallic fuel slug by oxidation, nitridation, or caburization of the metallic fuel slug. - In the fabricating method according to the present invention,
step 2 is a step of sealing the cladding tube after introducing the surface-treated metallic fuel slug into the cladding tube. - Formation of Oxide Protective Coating Layer
- A method of heat treating in a gas atmosphere containing oxygen, a method of dipping in an oxidation solution, and a method of performing an electrolytic treatment may be used as a method of forming an oxide protective coating layer.
- First, the method of heat treating in a gas atmosphere containing oxygen may be performed by heat treating a metallic fuel slug at a temperature ranging from 100° C. to 1000° C. and a pressure ranging from 1 atm to 50 atm in an atmosphere of oxygen, air, or inert gas containing oxygen.
- In the case that the heat treatment temperature is less than 100° C., the oxide layer may not be efficiently formed. In the case in which the heat treatment temperature is greater than 1000° C., transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded. Also, a pressurization treatment may be performed for the efficient heat treatment. In the case that the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- Next, the method of dipping in an oxidation solution may be performed by dipping a metallic fuel slug in a hydrochloric, sulfuric, nitric, sodium hydroxide, or potassium hydroxide solution, and heat treating the metallic fuel slug at a temperature ranging from 30° C. to 90° C. for 30 minutes to 5 hours.
- Finally, the method of performing an electrolytic treatment may be performed by plasma electrolytic oxidation, micro-arc oxidation, micro-arc discharge oxidation, spark anodizing, anodic spark deposition, micro-arc anodizing, micro plasma anodizing, micro plasma oxidation, and electro plasma oxidation of a metallic fuel slug.
- Formation of Nitride Protective Coating Layer
- A method of heat treating in a gas atmosphere containing nitrogen and an ion nitriding method may be used as a method of forming a nitride protective coating layer.
- First, the method of heat treating in a gas atmosphere containing nitrogen may be performed by heat treating a metallic fuel slug at a temperature ranging from 100° C. to 1000° C. and a pressure ranging from 1 atm to 50 atm in an atmosphere of nitrogen, ammonia, or inert gas containing nitrogen.
- In the case that the heat treatment temperature is less than 100° C., the nitride layer may not be efficiently formed. In the case in which the heat treatment temperature is greater than 1000° C., transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded. Also, a pressurization treatment may be performed for the efficient heat treatment. In the case that the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- Next, the ion nitriding method may be performed by using a method of applying a negative potential to an object to be ion-nitrided in a gas atmosphere containing nitrogen. The ion nitriding method may be completed by heat treating the object under conditions of a temperature ranging from 100° C. to 1000° C., a pressure ranging from 1 atm to 50 atm, and a potential ranging from 1 V to 1,000 V in an inert atmosphere containing nitrogen. In the case that the heat treatment temperature is less than 100° C., the nitride layer may not be efficiently formed. In the case in which the heat treatment temperature is greater than 1000° C., transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded. Also, a pressurization treatment may be performed for the efficient heat treatment. In the case that the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced. With respect to the applied potential, efficient ion nitridation may not be achieved at a potential of less than 1 V. Since an additional insulation treatment may be required at a potential of greater than 1,000 V, economic efficiency of the process may be reduced.
- Formation of Carbide Protective Coating Layer
- A method of heat treating in a gas atmosphere containing carbon may be used as a method of forming a carbide protective coating layer.
- The method of heat treating in a gas atmosphere containing carbon may be performed by heat treating a metallic fuel slug at a temperature ranging from 100° C. to 1000° C. and a pressure ranging from 1 atm to 50 atm in an atmosphere of carbon, methane, carbon dioxide, or carbon monoxide.
- In the case that the heat treatment temperature is less than 100° C., the carbide layer may not be efficiently formed. In the case in which the heat treatment temperature is greater than 1000° C., transformation of the metallic fuel slug may occur and thus, the performance of the metallic fuel slug as a fuel may be degraded. Also, a pressurization treatment may be performed for the efficient heat treatment. In the case that the pressure of the heat treatment is 50 atm or more, an additional sealing apparatus may be required, and thus, economic efficiency of the process may be reduced.
- Also, the present invention provides a method of fabricating a nuclear fuel rod for fast reactors including: coating a surface of metallic fuel powder with a single protective coating layer selected from the group consisting of an oxide layer, a nitride layer, and a carbide layer by oxidation, nitridation, or caburization of the metallic fuel powder (step 1); preparing a metallic fuel slug by forming the metallic fuel powder coated with the protective coating layer in step 1 (step 2); and sealing a cladding tube after introducing the metallic fuel slug prepared in
step 2 into the cladding tube (step 3). - Since the method of fabricating a nuclear fuel rod for fast reactors according to the present invention may form the protective coating layer on the surface of the metallic fuel powder, components of fuel, fission products, or impurities may be stabilized and various types of fuels may be fabricated. In particular, the coated metallic fuel powder may be formed in the form of a metallic fuel slug during the fabrication of the nuclear fuel rod for fast reactors and thus, the interdiffusion phenomenon between the metallic fuel slug and the cladding tube sealing the metallic fuel slug may be reduced.
- In the fabricating method according to the present invention,
step 1 is a step of forming the protective coating layer on the surface of the metallic fuel powder. Specifically, an oxide, nitride, or carbide coating layer may be formed on the surface of the metallic fuel powder by oxidation, nitridation, or caburization of the metallic fuel powder. Preferred conditions that may form the protective layers are as described in the above specification. - In the fabricating method according to the present invention,
step 2 is a step of preparing the metallic fuel slug by forming the metallic fuel powder. Specifically, a method of stacking the powder in a nuclear fuel rod composed of a cylindrical cladding tube, a method of sintering the powder by heat treating in a heat treatment furnace, and a method of forming a cylindrical sintered body by introducing the metallic fuel powder into a metal or ceramic matrix and heat treating. - In the fabricating method according to the present invention, step 3 is a step of sealing the cladding tube after introducing the metallic fuel slug into the cladding tube.
- As described above, the nuclear fuel rod for fast reactors that includes the surface treated metallic fuel slug and the cladding tube according to the present invention has an excellent effect of stabilizing components of the metallic fuel slug and fission products or impurities, because the interdiffusion between the metallic fuel slug and the cladding tube does not occur. Also, since the uniform coating on the surface of the metallic fuel slug may be facilitated and fabrication costs may be significantly reduced in comparison to a typical technique of using a functional material for preventing the interdiffusion at an inner surface of the cladding tube, it may be suitable for fabricating the nuclear fuel rod for fast reactors.
- Hereinafter, the present invention will be described in more detail according to examples. However, the following examples are provided for illustrative purposes only, and the scope of the present invention should not be limited thereto in any manner.
- An oxide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 600° C. and a pressure of 5 atm for 2 hours in an argon gas atmosphere containing 20% oxygen. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 1 hour in an air atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 1 hour in an air atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a hydrochloric acid solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a sulfuric acid solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a nitric acid solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a sodium hydroxide solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a potassium hydroxide solution at 50° C. for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug through plasma electrolytic oxidation by dipping the metallic fuel slug formed of U-10Zr, a nuclear fuel material, in a potassium hydroxide solution and a sodium hydroxide solution, and then applying a positive voltage of 200 V thereto. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro-arc oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro-arc discharge oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by spark anodizing of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by anodic spark deposition of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro-arc anodizing of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro plasma anodizing of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by micro plasma oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An oxide layer was formed on a surface of a metallic fuel slug by electro plasma oxidation of the metallic fuel slug formed of U-10Zr, a nuclear fuel material. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 800° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A nitride layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 2 atm for 2 hours in a 100% pure ammonia gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 800° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 500° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 300° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- An ion-nitrided layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into a mixed gas containing 80% nitrogen and 20% argon gas, and heat treating the metallic fuel slug at a temperature of 150° C. and a negative voltage of 200 V for 2 hours. Then, the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 700° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 500° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 300° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by introducing the metallic fuel slug formed of U-10Zr, a nuclear fuel material, into carbon powder and heat treating the metallic fuel slug at a temperature of 150° C. and a pressure of 1 atm for 2 hours. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 700° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 2 hours in a methane gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 700° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 2 hours in a carbon dioxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 700° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 500° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 300° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A carbide layer was formed on a surface of a metallic fuel slug by heat treating the metallic fuel slug formed of U-10Zr, a nuclear fuel material, at a temperature of 150° C. and a pressure of 1 atm for 2 hours in a carbon monoxide gas atmosphere. Then, the heat-treated metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- A surface treatment was not performed on a metallic fuel slug formed of U-10Zr, a nuclear fuel material, and the metallic fuel slug was put into a HT9 (12Cr-1Mo) cladding tube to fabricate a nuclear fuel rod for fast reactors.
- The following experiments were performed for evaluating the interdiffusivity between the metallic fuel slug and the cladding tube in the nuclear fuel rods for fast reactors fabricated in examples.
- Specifically, the nuclear fuel rods for fast reactors fabricated in Examples 1, 2, 3, and 18, and Comparative Example 1 were cut to a length of 10 mm, and the 10 mm long nuclear fuel rods were then cut in half in a radial direction. Then, metallic fuel slug-cladding tube diffusion couple experiments were performed at 800° C. for 25 hours. After the diffusion couple experiments, bonded samples were cooled and cross sections of the bonded samples were observed using a scanning electron microscope. The results thereof are presented in
FIGS. 2 to 6 . -
FIG. 2 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 1 of the present invention after the diffusion couple experiment. -
FIG. 3 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 2 of the present invention after the diffusion couple experiment. -
FIG. 4 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 3 of the present invention after the diffusion couple experiment. -
FIG. 5 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Example 18 of the present invention after the diffusion couple experiment. -
FIG. 6 is a scanning electron microscope image of the cross section of the nuclear fuel rod for fast reactors according to Comparative Example 1 of the present invention after the diffusion couple experiment. - As illustrated in
FIGS. 2 to 6 , with respect to Example 1 (FIG. 2 ), Example 2 (FIG. 3 ), Example 3 (FIG. 4 ), and Example 18 (FIG. 5 ), it was observed that the interactions between the metallic fuel slugs and the cladding tubes did not occur because dense oxide layers and nitride layer were formed on the surfaces of the metallic fuel slugs. In contrast, with respect to Comparative Example 1 (FIG. 6 ), it may be observed that the metallic fuel slug material and the cladding tube material were interdiffused and reacted during the diffusion couple experiment. - Therefore, the nuclear fuel rod for fast reactors that includes the surface treated metallic fuel slug and the cladding tube according to the present invention had an excellent effect of stabilizing components of the metallic fuel slug and fission products or impurities, because the interdiffusion between the metallic fuel slug and the cladding tube did not occur. Also, since the uniform coating on the surface of the metallic fuel slug may be facilitated and fabrication costs may be significantly reduced in comparison to a typical technique of using a functional material for preventing the interdiffusion at an inner surface of the cladding tube, it may be suitable for fabricating the nuclear fuel rod for fast reactors. Furthermore, according to the present invention, since a rare earth element, which is included on the surface of a metallic fuel fabricated by pyroprocessing to degrade the performance of the metallic fuel, may be transformed into a non-active compound, such as oxide, nitride, and carbide, the improvement of the performance of the metallic fuel and the extension of the lifetime of the metallic fuel may be expected.
- Although the preferred embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.
Claims (3)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16/394,322 US20200075182A1 (en) | 2013-01-18 | 2019-04-25 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR10-2013-0005989 | 2013-01-18 | ||
| KR20130005989 | 2013-01-18 | ||
| KR10-2013-0110624 | 2013-09-13 | ||
| KR1020130110624A KR101527804B1 (en) | 2013-01-18 | 2013-09-13 | Nuclear fuel rod for fast nuclear reactor having metallic fuel slugs coated with protective films and fabrication method thereof |
| US14/079,740 US9589680B2 (en) | 2013-01-18 | 2013-11-14 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US15/412,560 US20170140841A1 (en) | 2013-01-18 | 2017-01-23 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US16/394,322 US20200075182A1 (en) | 2013-01-18 | 2019-04-25 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
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| Application Number | Title | Priority Date | Filing Date |
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| US15/412,560 Division US20170140841A1 (en) | 2013-01-18 | 2017-01-23 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
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| US20200075182A1 true US20200075182A1 (en) | 2020-03-05 |
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| US14/079,740 Expired - Fee Related US9589680B2 (en) | 2013-01-18 | 2013-11-14 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US15/412,560 Abandoned US20170140841A1 (en) | 2013-01-18 | 2017-01-23 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US15/412,540 Abandoned US20170200514A1 (en) | 2013-01-18 | 2017-01-23 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US16/394,322 Abandoned US20200075182A1 (en) | 2013-01-18 | 2019-04-25 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
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| US14/079,740 Expired - Fee Related US9589680B2 (en) | 2013-01-18 | 2013-11-14 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US15/412,560 Abandoned US20170140841A1 (en) | 2013-01-18 | 2017-01-23 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
| US15/412,540 Abandoned US20170200514A1 (en) | 2013-01-18 | 2017-01-23 | Nuclear fuel rod for fast reactors including metallic fuel slug coated with protective coating layer and fabrication method thereof |
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| US (4) | US9589680B2 (en) |
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| JP6579842B2 (en) * | 2015-07-17 | 2019-09-25 | 日立Geニュークリア・エナジー株式会社 | Fuel element and fuel assembly for fast reactor and core loaded with the same |
| ES2827830T3 (en) * | 2016-09-28 | 2021-05-24 | Commissariat Energie Atomique | Nuclear component with metallic substrate, manufacturing process by DLI-MOCVD and uses against oxidation / hydriding |
| ES2776802T3 (en) | 2017-05-12 | 2020-08-03 | Westinghouse Electric Sweden Ab | Nuclear fuel pellet, fuel rod and fuel assembly |
| RU2733900C1 (en) * | 2020-03-06 | 2020-10-08 | Государственная корпорация по атомной энергии "Росатом" | Fast liquid-salt reactor |
| CN114267460B (en) * | 2021-12-22 | 2023-03-24 | 西安交通大学 | Plate-shaped fuel element for suppressing foaming phenomenon |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4071587A (en) * | 1975-09-25 | 1978-01-31 | General Atomic Company | Method of making ZrH fuel element |
| KR100285168B1 (en) | 1997-12-02 | 2001-03-15 | 장인순 | Manufacturing method of carbide, boride or nitride coated fuel using high temperature and high pressure combustion synthesis |
| JPH11202072A (en) | 1998-01-14 | 1999-07-30 | Toshiba Corp | Nuclear fuel particles, nuclear fuel pellets and nuclear fuel elements for nuclear reactors |
| KR100915602B1 (en) | 2007-08-17 | 2009-09-07 | 한국원자력연구원 | Nuclear fuel rod for high speed reactor with oxide coating layer on inner surface of coating tube |
| KR101032480B1 (en) | 2009-01-07 | 2011-05-03 | 한국수력원자력 주식회사 | Plating method of inner wall of nuclear fuel cladding and nuclear fuel cladding manufactured thereby |
| KR101038106B1 (en) | 2009-04-15 | 2011-06-01 | 한국수력원자력 주식회사 | Method of depositing functional multilayer thin film at low temperature on nuclear fuel cladding for high speed furnace |
| KR101209139B1 (en) | 2011-03-21 | 2012-12-06 | 한국수력원자력 주식회사 | Nitriding surface treated nuclear fuel powder and dispersion nuclear fuel having the same |
| JP2012237574A (en) | 2011-05-10 | 2012-12-06 | Yuji Uenohara | Cladding tube and nuclear reactor |
| KR101189169B1 (en) | 2011-10-10 | 2012-10-10 | 한국수력원자력 주식회사 | A method for preparing metallic fuel slugs of low loss and high yield, and metallic fuel slugs prepared by the method |
| KR101218774B1 (en) * | 2011-12-23 | 2013-01-09 | 한국원자력연구원 | Nuclear fuel rod for fast reactor |
-
2013
- 2013-11-14 US US14/079,740 patent/US9589680B2/en not_active Expired - Fee Related
-
2017
- 2017-01-23 US US15/412,560 patent/US20170140841A1/en not_active Abandoned
- 2017-01-23 US US15/412,540 patent/US20170200514A1/en not_active Abandoned
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2019
- 2019-04-25 US US16/394,322 patent/US20200075182A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20140205054A1 (en) | 2014-07-24 |
| US20170140841A1 (en) | 2017-05-18 |
| US20170200514A1 (en) | 2017-07-13 |
| US9589680B2 (en) | 2017-03-07 |
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