US20020181642A1 - Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding - Google Patents

Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding Download PDF

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Publication number
US20020181642A1
US20020181642A1 US09/871,972 US87197201A US2002181642A1 US 20020181642 A1 US20020181642 A1 US 20020181642A1 US 87197201 A US87197201 A US 87197201A US 2002181642 A1 US2002181642 A1 US 2002181642A1
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metal oxide
fuel
container
fuel rod
oxide
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US09/871,972
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Swaminathan Vaidyanathan
John Davies
Steven Wisner
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General Electric Co
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General Electric Co
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Priority to US09/871,972 priority Critical patent/US20020181642A1/en
Application filed by General Electric Co filed Critical General Electric Co
Assigned to GENERAL ELECTRIC COMPANY reassignment GENERAL ELECTRIC COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DAVIES, JOHN H., VAIDYANATHAN, SWAMINATHAN, WISNER, STEVEN B.
Priority to US10/098,563 priority patent/US20020181643A1/en
Priority to ES02253664.3T priority patent/ES2275811T5/en
Priority to DE60215886.9T priority patent/DE60215886T3/en
Priority to EP02253664.3A priority patent/EP1265256B2/en
Priority to JP2002161926A priority patent/JP4301540B2/en
Publication of US20020181642A1 publication Critical patent/US20020181642A1/en
Priority to US10/330,282 priority patent/US6697450B2/en
Priority to US10/345,167 priority patent/US20030133532A1/en
Abandoned legal-status Critical Current

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    • 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
    • G21C3/18—Internal spacers or other non-active material within the casing, e.g. compensating for expansion of fuel rods or for compensating excess reactivity
    • 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
    • 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 invention relates generally to an improved fuel rod design for use in nuclear reactors. More paticularly, the present invention provides nuclear reactor fuel rods in which one or more metal oxides are present within the fuel rod to mitigate secondary hydriding.
  • the present invention seeks to fill that need.
  • the invention is particularly directed to providing improved fuel rod design for use in a Light Water Reactor (LWR).
  • LWR Light Water Reactor
  • the invention provides a method of fabricating a fuel rod in which the tendency for secondary hydriding is mitigated, comprising the step of providing an effective amount of a metal oxide in the fuel rod.
  • the composition of the metal oxide is generally such that if the hydrogen fraction is above the equilibrium condition for the M/MOx couple, a back reaction occurs between the hydrogen and the metal oxide to generate steam and mitigate secondary hydriding.
  • the metal oxide may be selected from oxides of iron, nickel, tin, bismuth, copper, colbalt, chromium, manganese and/or combinations of such oxides.
  • the invention provides a fuel rod with reduced tendency to undergo secondary hydriding, fabricated according to the method of the invention.
  • FIG. 1 is a container with perforations or slits in the wall thereof;
  • FIG. 2 is a fuel rod with the metal oxide within the rod.
  • the present invention resides in the surprising discovery that secondary hydriding in nuclear reactor fuel rods can be sigificantly mitigated, and in some instances substantially eliminated, by providing in the interior of the fuel rod an effective amount of one or more metal oxides.
  • the oxides may be those of iron, nickel, tin, bismuth, copper, colbalt, chromium, manganese and/or combinations of such oxides.
  • suitable metal oxides are iron oxides (Fe 3 O 4 ; Fe 2 O 3 ), nickel oxide (NiO), tin oxide (SnO 2 ), copper oxide (CuO) and bismuth oxide (Bi 2 O 3 ).
  • the invention finds particular applcation to uranium oxide fuel contained within zirconium-alloy based cladding. Such fuel rods are commonly employed in LWRs.
  • the hydrogen:steam ratio within the rod in the region near the metal oxide will be dictated by the thermodynamic equilibrium for the Metal/Metal Oxide (M/MOx) couple, evaluated at the temperature within the fuel rod where the metal oxide is located. If the hydrogen fraction rises above the equilibrium condition for the M/MOx couple, back reaction between the hydrogen and MOx will generate steam and maintain the interior at the posited equilibrium.
  • M/MOx Metal/Metal Oxide
  • the ratio of steam to hydrogen in equilibrium with the metal oxide is such that the steam fraction is above the threshold level for secondary hydriding, secondary hydriding will be mitigated. Since the steam generated by the back reaction between the hydrogen and metal oxide can easily diffuse over a certain length, secondary hydriding can be mitigated even if the metal oxide is present only at discrete intervals.
  • the metal oxide may be present as a coating on the cladding interior surface.
  • the metal oxide may be selected from iron oxides (Fe 3 O 4 ; Fe 2 O 3 ), nickel oxide (NiO), tin oxide (SnO 2 ), copper oxide (CuO) and bismuth oxide (Bi 2 O 3 ).
  • Bismuth oxide is generally employed as it has a lower cross-section for absorption of neutrons than the other oxides.
  • the coating is applied to a thickness in the range of I mil (25 microns) or less, for example 0.25-0.5 mil.
  • the metal oxide may be present as a coating on the fuel pellet surfaces.
  • the metal oxide may be selected from iron oxides (Fe 3 O 4 ; Fe 2 O 3 ), nickel oxide (NiO), tin oxide (SnO 2 ), copper oxide (CuO) and bismuth oxide (Bi 2 O 3 ).
  • Bismuth oxide is generally employed as it has a lower cross-section for absorption of neutrons than the other oxides.
  • the coating is applied to a thickness in the range of I mil (25 microns) or less, for example 0.25-0.5 mil.
  • the metal oxide may be present as individual pellets or as wafers between fuel pellets, or at the bottom of the fuel stack or at the top of the fuel stack or combinations thereof.
  • the individual pellets or wafers will be of nearly the same geometry (diameter) as the pellet, possibly a little larger. In the instance where they are present between the fuel pellets, the pellet or wafer thickness will depend upon the number of pellets or wafers used.
  • the pellets or wafers are generally fabricated by sintering the metal oxide powder selected from iron oxides (Fe 3 O 4 ; Fe 2 O 3 ), nickel oxide (NiO), tin oxide (SnO 2 ), copper oxide (CuO) and bismuth oxide (Bi 2 O 3 ).
  • the metal oxide powder selected from iron oxides (Fe 3 O 4 ; Fe 2 O 3 ), nickel oxide (NiO), tin oxide (SnO 2 ), copper oxide (CuO) and bismuth oxide (Bi 2 O 3 ).
  • FIG. 1 shows a container 2 with perforations or slits 4 in the wall thereof which provide free access to the surrounding gases.
  • the container is typically fabricated of a material that does not react with the metal oxide, such as stainless steel.
  • the container wall has a thickness of 10 mils or less and an outside diameter which is essentially the same as fuel pellets, or slightly larger.
  • the metal oxide may be present in the container 2 as a powder or pellet, as described above.
  • the metal oxide may be discretely distributed (rather than in a continuous manner) along the fuel rod.
  • the metal oxide may be in any of the configurations described in the first through fourth embodiments above.
  • FIG. 2 there is shown a fuel rod 6 comprising an outer cladding 8 and a fuel pellet stack 10 .
  • a container 2 as described above, is provided at the bottom of and retained in place by bottom end cap 12 and the fuel stack 10 containing metal oxide.
  • FIG. 2 illustrates the situation where the container is at the bottom of the fuel stack.
  • a similar container may also be placed at the top of the fuel stack.
  • a container is placed at the bottom of the fuel stack, and a further container may optionally be present at the top of the stack.
  • a plenum and a retainer spring (not shown) which presses down on the container to hold it in place.
  • the specific metal oxide to be used for secondary hydriding mitigation may be selected from the oxides of Ni, Fe, Sn, Bi, Cu, Co, Cr, and Mn.
  • the metal oxide is typically present in each fuel rod in an amount of up to about 15 grams, more usually up to about 12 grams, for example 2 to 10 grams.
  • the specific metal oxide to be chosen is to be based on whether the metal oxide reacts with hydrogen rapidly enough.
  • the rapidity of this reaction must be such that the rate is sufficiently fast so that it can counteract the rate at which hydrogen is produced in the forward reaction.
  • a further factor in the choice of metal oxide is whether the equilibrium hydrogen:steam ratio is sufficiently rich in steam to avert secondary hydriding. Generally, if the pressure of steam is greater than about 5% of the hydrogen pressure, it is believed that hydriding can be avoided.
  • the oxides of iron, nickel, tin, bismuth and copper are employed.
  • Bismuth oxide (Bi 2 O 3 ) is typically employed when the metal oxide is to be placed in the fuel pellet column space as it minimizes parasitic neutron absorption from the introduction of metal oxide into the core.
  • Copper oxide (CuO) is typically employed when the metal oxide is to be located at the bottom or at the top of the fuel column where parasitic neutron absorption is not a prime consideration. Oxides of specific isotopes of these materials that minimize parasitic absorption may also be employed.

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Monitoring And Testing Of Nuclear Reactors (AREA)
  • Catalysts (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

Method of fabricating a fuel rod, comprising providing an effective amount of a metal oxide in the fuel rod to generate steam and mitigate the tendency for secondary hydriding. Fuel rods fabricated according to the method of the invention are also provided.

Description

  • The present invention relates generally to an improved fuel rod design for use in nuclear reactors. More paticularly, the present invention provides nuclear reactor fuel rods in which one or more metal oxides are present within the fuel rod to mitigate secondary hydriding. [0001]
    • BACKGROUND OF THE INVENTION
  • When an LWR fuel rod cladding is breached, for example as a result of debris fretting, the coolant water/steam ingresses to the interior of the fuel rod where an oxidation reaction occurs with the fuel and zirconium alloy cladding to produce hydrogen and zirconium and uranium oxide moieties. The net effect of this oxidation reaction is that the oxygen in the steam is progressively removed and the interior space of the fuel rod is filled with a mixture of hydrogen and steam. At a sufficient distance from the primary breach location, the hydrogen is extremely dry, as most of the steam has been reacted out. Under these conditions, the hydrogen is rapidly absorbed by the cladding to form massive secondary hydrides which are brittle in nature. Subsequent loading of the cladding leads to a new rupture at these secondary hydrided locations. The rupture may be cirucumferential or, in some instances, could lead to axial crack propagation. In all cases, there is additional exposure of the fuel and fission products to the coolant. For this reason, it is important to mitigate secondary hydriding of the cladding. [0002]
  • The conditions that relate to the formation of secondary hydrides in zirconium-alloy cladding have been discussed extensively in the literature. It is now well-recognized that massive secondary hydriding takes place when the steam fraction in the steam-hydrogen mixture interior to the cladding falls below a threshold level. Very dry hydrogen conditions are generally needed for massive secondary hydriding of the cladding, and even small quantities of steam will serve to mitigate secondary hydriding. [0003]
  • A need exists for a fuel rod design which will not be susceptible to secondary hydriding of zirconium-alloy fuel cladding in the event of cladding breach and ingress of water or steam to the interior of the fuel rod. The present invention seeks to fill that need. [0004]
    • SUMMARY OF THE INVENTION
  • It has now been discovered, surprisingly, that secondary hydriding can be mitigated or eliminated by providing one or more metal oxides within the fuel rod. The invention is particularly directed to providing improved fuel rod design for use in a Light Water Reactor (LWR). [0005]
  • In a first aspect, the invention provides a method of fabricating a fuel rod in which the tendency for secondary hydriding is mitigated, comprising the step of providing an effective amount of a metal oxide in the fuel rod. The composition of the metal oxide is generally such that if the hydrogen fraction is above the equilibrium condition for the M/MOx couple, a back reaction occurs between the hydrogen and the metal oxide to generate steam and mitigate secondary hydriding. The metal oxide may be selected from oxides of iron, nickel, tin, bismuth, copper, colbalt, chromium, manganese and/or combinations of such oxides. [0006]
  • In a further aspect, the invention provides a fuel rod with reduced tendency to undergo secondary hydriding, fabricated according to the method of the invention.[0007]
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • The invention will now be described with reference to the accompanying drawings, in which: [0008]
  • FIG. 1 is a container with perforations or slits in the wall thereof; and [0009]
  • FIG. 2 is a fuel rod with the metal oxide within the rod.[0010]
    • DETAILED DESCRIPTION OF THE INVENTION
  • The present invention resides in the surprising discovery that secondary hydriding in nuclear reactor fuel rods can be sigificantly mitigated, and in some instances substantially eliminated, by providing in the interior of the fuel rod an effective amount of one or more metal oxides. The oxides may be those of iron, nickel, tin, bismuth, copper, colbalt, chromium, manganese and/or combinations of such oxides. Specific examples of suitable metal oxides are iron oxides (Fe[0011] 3O4; Fe2O3), nickel oxide (NiO), tin oxide (SnO2), copper oxide (CuO) and bismuth oxide (Bi2O3). The invention finds particular applcation to uranium oxide fuel contained within zirconium-alloy based cladding. Such fuel rods are commonly employed in LWRs.
  • When steam enters the interior of the fuel cladding, an oxidation reaction occurs with the fuel/cladding which results in the generation of hydrogen. This may be described generally as follows: [0012]
  • xH2O+Zr=ZrOx+xH2
  • xH2O+UO2=UO2+X+xH2
  • The hydrogen:steam ratio within the rod in the region near the metal oxide will be dictated by the thermodynamic equilibrium for the Metal/Metal Oxide (M/MOx) couple, evaluated at the temperature within the fuel rod where the metal oxide is located. If the hydrogen fraction rises above the equilibrium condition for the M/MOx couple, back reaction between the hydrogen and MOx will generate steam and maintain the interior at the posited equilibrium. [0013]
  • It is to be noted that in some instances the equilibrium could correspond to a couple such as MOz/MOx where MOz is a lower oxide, that is z<x, and not pure metal. The back reaction is therefore described as follows: [0014]
  • MOx+H2=M (or MOz, z<x)+H2O
  • Provided the ratio of steam to hydrogen in equilibrium with the metal oxide is such that the steam fraction is above the threshold level for secondary hydriding, secondary hydriding will be mitigated. Since the steam generated by the back reaction between the hydrogen and metal oxide can easily diffuse over a certain length, secondary hydriding can be mitigated even if the metal oxide is present only at discrete intervals. [0015]
  • The presence of metal oxide may be in accordance with several possible embodiments. In a first embodiment, the metal oxide may be present as a coating on the cladding interior surface. The metal oxide may be selected from iron oxides (Fe[0016] 3O4; Fe2O3), nickel oxide (NiO), tin oxide (SnO2), copper oxide (CuO) and bismuth oxide (Bi2O3). Bismuth oxide is generally employed as it has a lower cross-section for absorption of neutrons than the other oxides. Generally, the coating is applied to a thickness in the range of I mil (25 microns) or less, for example 0.25-0.5 mil.
  • As a second embodiment, the metal oxide may be present as a coating on the fuel pellet surfaces. The metal oxide may be selected from iron oxides (Fe[0017] 3O4; Fe2O3), nickel oxide (NiO), tin oxide (SnO2), copper oxide (CuO) and bismuth oxide (Bi2O3). Bismuth oxide is generally employed as it has a lower cross-section for absorption of neutrons than the other oxides. Generally, the coating is applied to a thickness in the range of I mil (25 microns) or less, for example 0.25-0.5 mil.
  • As a third embodiment, the metal oxide may be present as individual pellets or as wafers between fuel pellets, or at the bottom of the fuel stack or at the top of the fuel stack or combinations thereof. Generally, the individual pellets or wafers will be of nearly the same geometry (diameter) as the pellet, possibly a little larger. In the instance where they are present between the fuel pellets, the pellet or wafer thickness will depend upon the number of pellets or wafers used. The pellets or wafers are generally fabricated by sintering the metal oxide powder selected from iron oxides (Fe[0018] 3O4; Fe2O3), nickel oxide (NiO), tin oxide (SnO2), copper oxide (CuO) and bismuth oxide (Bi2O3).
  • As a fourth embodiment, reference is made to the accompanying FIG. 1 showing a [0019] container 2 with perforations or slits 4 in the wall thereof which provide free access to the surrounding gases. The container is typically fabricated of a material that does not react with the metal oxide, such as stainless steel. The container wall has a thickness of 10 mils or less and an outside diameter which is essentially the same as fuel pellets, or slightly larger. The metal oxide may be present in the container 2 as a powder or pellet, as described above.
  • In a fifth embodiment, the metal oxide may be discretely distributed (rather than in a continuous manner) along the fuel rod. The metal oxide may be in any of the configurations described in the first through fourth embodiments above. [0020]
  • In a sixth embodiment, referring to FIG. 2, there is shown a [0021] fuel rod 6 comprising an outer cladding 8 and a fuel pellet stack 10. A container 2 as described above, is provided at the bottom of and retained in place by bottom end cap 12 and the fuel stack 10 containing metal oxide. FIG. 2 illustrates the situation where the container is at the bottom of the fuel stack. However, a similar container may also be placed at the top of the fuel stack. In the usual arrangement, a container is placed at the bottom of the fuel stack, and a further container may optionally be present at the top of the stack. When a container is at the top of the fuel stack, there is a plenum and a retainer spring (not shown) which presses down on the container to hold it in place.
  • The specific metal oxide to be used for secondary hydriding mitigation may be selected from the oxides of Ni, Fe, Sn, Bi, Cu, Co, Cr, and Mn. The metal oxide is typically present in each fuel rod in an amount of up to about 15 grams, more usually up to about 12 grams, for example 2 to 10 grams. [0022]
  • The specific metal oxide to be chosen is to be based on whether the metal oxide reacts with hydrogen rapidly enough. The rapidity of this reaction must be such that the rate is sufficiently fast so that it can counteract the rate at which hydrogen is produced in the forward reaction. [0023]
  • A further factor in the choice of metal oxide is whether the equilibrium hydrogen:steam ratio is sufficiently rich in steam to avert secondary hydriding. Generally, if the pressure of steam is greater than about 5% of the hydrogen pressure, it is believed that hydriding can be avoided. [0024]
  • Generally, the oxides of iron, nickel, tin, bismuth and copper are employed. Bismuth oxide (Bi[0025] 2O3) is typically employed when the metal oxide is to be placed in the fuel pellet column space as it minimizes parasitic neutron absorption from the introduction of metal oxide into the core. Copper oxide (CuO) is typically employed when the metal oxide is to be located at the bottom or at the top of the fuel column where parasitic neutron absorption is not a prime consideration. Oxides of specific isotopes of these materials that minimize parasitic absorption may also be employed.
    • EXAMPLE
  • The following example serves to illustrate the present invention. [0026]
  • Tests have been conducted where a zirconium strip was placed in a confined space within a stainless stell container and hydrogen admitted to the confined space through a very small hole in the container. The strip was shown to be massively hydrided within one day at 400° C. However, when specific metal oxides were present within the confined space, in addition to the zirconium strip, no hydriding was evident when tested under the same configuration and test conditions. The tests were conducted with Fe[0027] 2O3, Fe3O4, CuO, Bi2O3, NiO and SnO2.
  • While the invention has been described in connection with what is presently considered to be the most practical and preferred embodiment, it is to be understood that the invention is not to be limited to the disclosed embodiment, but on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims. [0028]

Claims (19)

What is claimed is:
1. A method of fabricating a fuel rod, comprising the step of providing an effective amount of a metal oxide in the fuel rod to cause generation of steam and mitigate secondary hydriding.
2. A method according to claim 1, wherein the composition of the metal oxide is such that if hydrogen fraction is above the equilibrium condition for the metal/metal oxide couple, a back reaction occurs between the hydrogen and the metal oxide to generate steam.
3. A method according to claim 1, wherein the metal oxide is selected from oxides of iron, nickel, tin, bismuth, copper, colbalt, chromium, manganese and combinations of such oxides.
4. A method according to claim 3, wherein the metal oxide is bismuth oxide.
5. A method according to claim 1, wherein the metal oxide is present in an amount ranging from up to 10 grams per fuel rod.
6. A method according to claim 1, wherein the metal oxide is present as a coating on an interior surface of cladding of the fuel rod.
7. A method according to claim 1, wherein the metal oxide is present as a coating on fuel pellet surfaces.
8. A method according to claim 1, wherein the metal oxide is present as individual pellets as a fuel pellet stack, or as wafers.
9. A method according to claim 8, wherein the individual pellets or wafers are between fuel pellet s.
10. A method according to claim 8, wherein the individual pellets or wafers are at the top of the fuel pellet stack.
11. A method according to claim 8, wherein the individual pellets or wafers are at the bottom of the fuel pellet stack.
12. A method according to claim 8, wherein the individual pellets or wafers are at the top and bottom of the fuel pellet stack.
13. A method according to claim 1, wherein the metal oxide is within a container.
14. A method according to claim 13, wherein the metal oxide is present as a powder or pellet within said container.
15. A method according to claim 13, wherein said container is at the bottom of a fuel pellet stack.
16. A method according to claim 13, wherein said container is at the top of a fuel pellet stack.
17. A method according to claim 13, wherein said container is at the top and bottom of a fuel pellet stack.
18. A method according to claim 1, wherein the metal oxide is distributed intermittently along the fuel rod.
19. A fuel rod fabricated according to the method of claim 1.
US09/871,972 2001-06-04 2001-06-04 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding Abandoned US20020181642A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
US09/871,972 US20020181642A1 (en) 2001-06-04 2001-06-04 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
US10/098,563 US20020181643A1 (en) 2001-06-04 2002-03-18 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
ES02253664.3T ES2275811T5 (en) 2001-06-04 2002-05-24 Zirconium alloy sheathed fuel rods containing metal oxide for secondary hybridization attenuation
DE60215886.9T DE60215886T3 (en) 2001-06-04 2002-05-24 Fuel rod with a shell of a zirconium alloy and containing a metal oxide for limiting the hydrogenation
EP02253664.3A EP1265256B2 (en) 2001-06-04 2002-05-24 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
JP2002161926A JP4301540B2 (en) 2001-06-04 2002-06-03 Fuel rod and manufacturing method thereof
US10/330,282 US6697450B2 (en) 2001-06-04 2002-12-30 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
US10/345,167 US20030133532A1 (en) 2001-06-04 2003-01-16 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding

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US09/871,972 US20020181642A1 (en) 2001-06-04 2001-06-04 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding

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US10/098,563 Continuation US20020181643A1 (en) 2001-06-04 2002-03-18 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
US10/330,282 Continuation US6697450B2 (en) 2001-06-04 2002-12-30 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding

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US10/098,563 Abandoned US20020181643A1 (en) 2001-06-04 2002-03-18 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
US10/330,282 Expired - Fee Related US6697450B2 (en) 2001-06-04 2002-12-30 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
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US10/330,282 Expired - Fee Related US6697450B2 (en) 2001-06-04 2002-12-30 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding
US10/345,167 Abandoned US20030133532A1 (en) 2001-06-04 2003-01-16 Zirconium-alloy clad fuel rods containing metal oxide for mitigation of secondary hydriding

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WO2013191743A1 (en) * 2012-02-17 2013-12-27 The Massachusetts Institute Of Technology Surface modification of cladding material
CN106663475A (en) * 2014-04-14 2017-05-10 先进核反应堆概念有限责任公司 Ceramic nuclear fuel dispersed in metallic alloy matrix

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SE532185C2 (en) * 2007-04-10 2009-11-10 Westinghouse Electric Sweden Method of operating a reactor at a nuclear plant
JP4909951B2 (en) * 2008-07-14 2012-04-04 株式会社東芝 Neutron shield
US9666310B1 (en) 2013-03-19 2017-05-30 U.S. Department Of Energy Accident-tolerant oxide fuel and cladding
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JP4301540B2 (en) 2009-07-22
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DE60215886D1 (en) 2006-12-21
DE60215886T2 (en) 2007-09-06
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EP1265256B2 (en) 2015-12-09
US20030133532A1 (en) 2003-07-17
ES2275811T3 (en) 2007-06-16
DE60215886T3 (en) 2016-04-28

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