GB2050206A - Nuclear fuel element cladding - Google Patents

Nuclear fuel element cladding Download PDF

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Publication number
GB2050206A
GB2050206A GB8000027A GB8000027A GB2050206A GB 2050206 A GB2050206 A GB 2050206A GB 8000027 A GB8000027 A GB 8000027A GB 8000027 A GB8000027 A GB 8000027A GB 2050206 A GB2050206 A GB 2050206A
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Prior art keywords
cladding tube
zirconium
tube
composite
zirconium alloy
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GB2050206B (en
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General Electric Co
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General Electric Co
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    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21CNUCLEAR REACTORS
    • G21C3/00Reactor fuel elements and their assemblies; Selection of substances for use as reactor fuel elements
    • G21C3/02Fuel elements
    • G21C3/04Constructional details
    • G21C3/16Details of the construction within the casing
    • G21C3/20Details 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
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/30Nuclear fission reactors

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Pressure Welding/Diffusion-Bonding (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
  • Extrusion Of Metal (AREA)
  • Rigid Pipes And Flexible Pipes (AREA)
  • Laminated Bodies (AREA)

Abstract

Composite cladding 12 for a nuclear fuel element containing fuel pellets 13 is formed with a zirconium metal barrier layer 22 bonded a to the inside surface of a zirconium alloy tube 21. The composite tube is sized by a cold working tube reduction process and is heat treated after final reduction to provide complete recrystallization of the zirconium metal barrier layer and a fine- grained microstructure. The zirconium alloy tube is stress-relieved but is not fully recrystallized. The crystallographic structure of the zirconium metal barrier layer may be improved by compressive deformation such as shot-peening. <IMAGE>

Description

SPECIFICATION Thermal-mechanical treatment of composite nuclear fuel element cladding Water cooled and moderated nuclear power reactors are well-known and are discussed, for example, by M. M. El-Wakil in "Nuclear Power Engineering" McGraw-Hill Book Com- pany, Inc., 1962.
Fuel elements for such reactors typically are in the form of uranium oxide and/or plutonium oxide pellets contained in a protective, elongated cladding tube formed of a suitable metal, commonly a zirconium alloy such as Zircaloy-2. Such a fuel element is shown, for example, in U.S. Patent No. 3,365,371.
To prevent premature failure of the fuel element cladding and to extend its useful mechanical life, various protective barriers between the column of fuel pellets and the inner surface of the cladding have been proposed.
Among these barriers are layers of zirconium metal bonded to the inner surface of the zirconium alloy of the cladding tube.
In Belgian Patent 835,481, there is described a barrier layer formed of substantially pure zirconium metal bonded to the inner surface of the cladding tube.
In Belgian Patent 8'70,342, there is described a barrier layer formed of zirconium metal of moderate purity such as sponge zirconium.
In the conventional process for producing cladding tubing with a barrier layer bonded to the inside surface thereof, a hollow billet of zirconium alloy is fitted with a sleeve of the zirconium metal for the barrier layer and the composite is co-extruded. The composite is then reduced to final diameters by cold working by multiple passes through a reduction device such as a pilger tube reduction machine.
After each reduction pass it is conventional to anneal the composite by heat treatment at a temperature and for a time period sufficient to substantially fully recrystallize the zirconium alloy.
However, it is found that the annealing temperatures and times needed for full recrystallization of the zirconium alloy cause undesirable grain growth in the zirconium metal barrier layer.
The present invention provides a method of making an elongated composite cladding tube for containing nuclear fuel as a fuel element for a nuclear reactor, said cladding tube being formed from a cladding tube shell comprised of a zirconium alloy tube containing constituents other than zirconium in an amount greater than about 5000 parts per million and having a layer of zirconium metal containing impurities of less than 500 parts per million metallurgically bonded to the inside surface thereof, comprising the steps of:: (1) reducing the diameter of said cladding tube shell by cold working in a series of reduction steps to the desired inside diameter and wall thickness; (2) heat treating said cladding tube shell between each of said reduction steps at a temperature and for a time period sufficient to substantially fully recrystallize said zirconium alloy; (3) heat treating said cladding tube after the final one of said reduction steps at a lower temperature and for a time period which allows substantially complete recrystallization of said zirconium metal layer and provides a finegrained microstructure therein and which stress-relieves but does not fully recrystallize said zirconium alloy.
In accordance with one aspect of the invention, the crystallographic texture of the zircon- ium metal layer, optionally, can be improved by compressive deformation of the surface of the layer, for example, by shot-peening, without deformation of the zirconium alloy of the composite tubing.
The present invention also provides an elongated composite cladding tube for containing nuclear fuel as a fuel element for a nuclear reactor, said composite cladding tube comprising a zirconium alloy tube containing constituents other than zirconium in an amount greater than 5000 parts per million and having a layer of zirconium metal containing impurities of less than 500 parts per million metallurgically bonded to the inside surface thereof, said zirconium metal layer being substantially fully recrystallized to provide a finegrained microstructure therein, and said zirconium alloy tube being substantially fully stress-relieved but not fully recrystallized.
The present invention will be further described by way of example only with reference to the accompanying drawings in which: Figure 1 is a partly cutaway elevation view of a nuclear fuel element; Figure 2 is a transverse cross section view of the fuel element of Fig. 1; and Figure 3 is a chart of an example tube reduction and treatment method in accordance with the invention.
A nuclear fuel element 11, as illustrated in Figs. 1 and 2, comprises an elongated composite cladding tube 1 2 containing a column of fuel pellets 1 3 and it is sealed at its ends by lower and upper end plugs 14 and 1 6.
A plenum space 1 7 is provided to allow longitudinal expansion of the fuel and to provide space for gases released from the fuel during operation in the reactor. A spring 1 8 between the top of the fuel column and the upper end plug 1 6 retains the fuel column in position. As best shown in Fig. 2, the composite cladding tube 11 is sized with respect to the diameter of the fuel pellets to provide an annular clearance space or gap 1 9 between the fuel pellets and the inner surface of the cladding tube.
In a preferred embodiment of the invention, the composite cladding tube 11 includes a cladding tube 21 formed of a zirconium alloy and a barrier layer 22 of zirconium metal metallurgically bonded to the inner surface of the tube 21.
Among the zirconium alloys suitable for tube 21 are Zircaloy-2 and Zircaloy-4. Zircaloy-2 contains, on a weight basis, about 1.5 percent tin, 0.12 percent iron, 0.09 percent chromium, 0.005 percent nickel and the balance zirconium. Zircaloy-4 has less nickel than Zircaloy-2 but contains slightly more iron. In either case the alloy contains constituents other than zirconium in an amount greater than 5,000 parts per million.
The barrier layer 22, which may comprise from about 1 to about 30 percent of the thickness of the composite cladding, is formed of zirconium metal of limited impurity content ranging from high purity or substantially pure zirconium of less than 500 parts per million (ppm) impurities to an impurity content of up to 5,000 ppm but preferably of impurity content of less than about 4,200 ppm.
Of the impurities, oxygen content should be minimized and kept within a range of 200 ppm or less to a maximum of about 1,200 ppm. Other impurities may be within the normal range for commercial reactor grade sponge zirconium and are listed as follows: aluminum-75 ppm or less; boron-0.4 ppm or less; cadmium-0.4 ppm or less; carbon-270 ppm or less; chromium-200 ppm or less; cobalt-20 ppm or less; copper-50 ppm or less; hafnium-100 ppm or less; hydrogen-25 ppm or less; iron-1500 ppm or less; magnesium-20 ppm or iess; mangan ese-50 ppm or less; molybdenum-50 ppm or less; nickel-70 ppm or less; niobium-100 ppm or less; nitrogen-80 ppm or less; silicon-120 ppm or less; tin-50 ppm or less; tungsten-100 ppm or less; titanium-50 ppm or less; and uranium-3.5 ppm or less.
The zirconium metal barrier layer 22 is metallurgically bonded to the zirconium alloy tube 21 with sufficient cross diffusion therebetween to form a strong bond but with insufficient diffusion to contaminate the barrier layer 22 more than about one-half to one mil from the bond interface.
It is found that a zirconium metal barrier layer of in the order of 5 to 1 5 percent of the thickness of the composite cladding, and of a particularly preferred thickness of about 10 percent, prevents exposure of the zirconium alloy of the cladding tube 21 to the corrosive fission products.
The barrier layer also separates the zirconium alloy cladding tube from direct mechanical interaction with the fuel pellets and reduces the stresses that can result therefrom The barrier layer is found to maintain its desirable structural properties such as yield strength and hardness at levels considerably lower than those of conventional zirconium alloys.'ln effect, the metal barrier does not harden as much as conventional zirconium alloys when subjected to irradiation and this, together with its initially low yield strength, enables the metal barrier to deform plastically and relieve pellet-induced stresses in the fuel element during power transients.Pellet induced stresses in the fuel element can be brought about, for example, by swelling of the pellets of nuclear fuel at reactor operating temperatures so that the pellet comes into contact with the cladding.
The composite cladding of this invention can be fabricated by any of the following methods.
In one method a hollow tube of the zirconium metal selected to be the barrier layer is inserted into a hollow billet of the zirconium alloy selected to form the cladding tube. The assembly then is subjected to exposure bonding of the tube to the billet. The composite is extruded at elevated temperature of about 1000 to about 1400"F (about 538 to about 760"C) using conventional tube shell extrusion techniques. The extruded composite is then subjected to a process involving conventional tube reduction until the desired size of the composite cladding is achieved.
In another method, a hollow tube of the zirconium metal selected to be the barrier layer is inserted into a hollow billet of the zirconium alloy selected to form the cladding tube. The assembly then is subjected to a heating step, such as at 1400"F (760"C) for about 8 hours, to produce diffusion bonding between the zirconium metal tube and the billet. The composite is then extruded using conventional tube shell extrusion techniques and the extruded composite is subjected to a process involving conventional tube reduction until the desired size of cladding is achieved.
In still another method, a hollow tube of the zirconium metal selected to be the barrier layer is inserted into a hollow billet of the zirconium alloy selected to form the cladding tube. This assembly then is extruded using conventional tube shell extrusion techniques.
Then the extruded composite is subjected to a process involving conventional tube reduction until the desired size of cladding is achieved.
The dimensions of the starting materials are determined by ratios of the cross sectional areas of the barrier layer and the zirconium alloy portions of the desired composite cladding product. For example, the total cross sectional area of the final cladding is given by ATF = II/4 (ODTF IDTF ), where ATF is the area of the final product, ODTF is the outer diameter of the final product, and IDTF is the inner diameter of the final product. The cross sectional area of the de sired barrier is given by ABF = tri/4 (ODBF2IDBF2), where ABF is cross sectional area of the metal barrier, ODBF is outer diameter of the metal barrier, and IDBF is the inner diameter of the metal barrier.The total cross section of the initial billet of the cladding tube is given by ATI = II/4 (ODT,2IDT,2) where ATI is the total cross sectional area of the initial billet including the metal barrier, ODT, is the outer diameter of the initial billet, and IDT, is the inner diameter of the initial billet. The required cross sectional area of the initial barrier is determined by
Example An example of making a composite cladding tube 11 in accordance with the invention is as follows.
A billet for the zirconium alloy cladding tube and the insert for the zirconium metal barrier layer are machined, cleaned and assembled by standard procedures, the dimensions being selected for extrusion of the composite assembly in a hot extrusion press. The billet for the cladding tube consists of normal Zircaloy-2 alloy conforming to ASTM B353, Grade RA- 1 and the insert for the barrier layer consists of zirconium metal with impurity content within the limits set forth hereinbefore. The bores of the billet and insert are formed with an 8 mii per inch taper and pressed together to ensure good contact between the mating surfaces.
Example dimensions of the machined parts are as follows: for the cladding tube billet-9.0 in length, 5.74 in outside diameter, 2.44 in inside diameter; for the barrier layer insert-2.44 in outside diameter, 1.66 in inside diameter.
Prior to assembly, the mating surfaces of the billet and insert are lightly etched to remove traces of impurities. A suitable etchant is a solution of 70ml H2O, 30ml HNO3 (70% AQ) and 5ml HF (48% AQ).
To assure a satisfactory bond during extrusion the assembly may be pre-bonded by pressing the tapered insert into the tapered bore of the billet in a vacuum 620jum of mercury while maintaining a temperature of about 1400"F (760"C) for 8 hours with initial pressing forces of 30-45,000 Ibis this is found to provide bonding over 20-25 percent of the interface area.
To reduce end losses during extrusion, 2 inch long pieces of Zircaloy-2 may be welded to each end of the pre-bonded assembly and machined flush.
The extrusion of the pre-bonded billet assembly into a cladding tube shell is accomplished using the following parameters: extrusion rate-6 in/min, reduction ratio-6:1, tem perature-1 100'F and extrusion force-3500 tons.
All billet surfaces except the bore and floating mandrel may be lubricated with a water soluble lubricant baked on at 1300"F for 1 hour. After extrusion both ends of the tube shell are cut clean from the added end pieces and the inner surface honed to remove any surface flawa and improve the finish.
The final reduction of the composite tube shell to tubing of suitable size for fuel element cladding is accomplished by cold working in three passes through a well-known pilger tube reduction machine with heat treatment and cleaning between passes. The steps of a representative reduction process are set forth in Fig. 3.
The reduction process is conventional except for the modifications according to the subject invention. The basis for these modifications and the beneficial results obtained thereby will now be discussed.
The severe cold working that takes place in the tube reduction passes results in distortion of the shapes of the metal crystallites and produces many crystal defects within the crystallites. Thus cold worked metals are in a relatively high energy state which is not thermally stable. The process of metallurgical annealing uses heat to impart mobility to the atoms of the metal and allows them to rearrange themselves into a lower energy configuration, such annealing being a function of both temperature and time with temperature being the more sensitive parameter. In general the annealing temperature and time are selected to be sufficient to provide substantially complete recrystallization but insufficient to allow excessive crystal or grain growth.
Thus for the annealing steps (5) and (8) of the reduction process of Fig. 3, the temperatures and times are selected to provide substantially complete recrystallization of the zirconium alloy of the tube 21.
However, the relatively purer metal of the barrier layer 22 recrystallizes at a lower temperature and it is found that the conventional annealing temperatures and times suitable for the zirconium alloy, as in steps (5) and (8), causes grain growth in the barrier layer metal to an extent undesirable in the finished product.
Therefore in accordance with one aspect of the invention, after the final reduction pass the composite tube is heat treated at a lower temperature as shown in step (12).
Thus the temperature and time of the heat treatment of step (12) are selected such that the zirconium metal of the barrier layer 22 is substantially fully recrystallized without grain growth. This provides a barrier layer with a fine grained equi-axed microstructure with improved strength and ductility, increased resistance to stress corrosion cracking and high plastic stability.
The temperature and time of the heat treatment step (12) are also selected in consideration of providing full stress relief but not full recrystallization of the zirconium alloy of tube 21. This results in the additional advantage that the zirconium alloy retains the elongated grain structure imparted by the reduction process and has higher strength at high strain rates while still being relieve of internal stresses.
Suitable temperatures and times for the annealing steps (2), (5) and (8) are in ranges from about 1000"F (538 C) to 1300"F (704 C) for about 1-15 hours and preferably for about 1-4 hours.
Suitable temperatures and times for heat treatment step (12) are in ranges from about 825-950 F (440-510 C) for about 1-4 hours.
In accordance with another aspect of the invention the crystallographic texture (that is, the degree of preferred crystallographic orientation) of the zirconium metal barrier layer, optionally can be improved by mechanical, compressive deformation of the surface thereof. For example, before the final heat treatment step (12) the barrier layer can be shotpreened from inside the assembly to provide compressive deformation of this layer without significant deformation of the zirconium alloy tube.
Such mechanical treatment prior to final heat treatment, shown as step (10) in Fig. 3 provides improved crystallographic structure with basal poles (0002) strongly aligned in the radial direction of the composite cladding tube.

Claims (11)

1. A method of making an elongated composite cladding tube for containing nuclear fuel as a fuel element for a nuclear reactor, said cladding tube being formed from a cladding tube shell comprised of a zirconium alloy tube containing constituents other than zirconium in an amount greater than about 5000 parts per million and having a layer of zirconium metal containing impurities of less than 500 parts per million metallurgically bonded to the inside surface thereof, comprising the steps of:: (1) reducing the diameter of said cladding tube shell by cold working in a series of reduction steps to the desired inside diameter and wall thickness; (2) heat treating said cladding tube shell between each of said reduction steps at a temperature and for a time period sufficient to substantially fully recrystallize said zirconium alloy; (3) heat treating said cladding tube after the final one of said reduction steps at a lower temperature and for a time period which allows substantially complete recrystallization of said zirconium metal layer and provides a finegrained microstructure therein and which stress-relieves but does not fully recrystallize said zirconium alloy.
2. A method as claimed in claim 1 wherein the temperature and time of step (2) are from 538"C to 704"C and from 1 hour to 1 5 hours, respectively and wherein the temperature and time of step (3) are from 440"C to 510"C and from 1 hour to 4 hours, respectively.
3. A method as claimed in any one of claims 1 to 3 including the further step of substantially uniformly compressively deforming the surface of said zirconium metal layer before the heat treatment step (3).
4. A method as claimed in claim 3 wherein said deforming is accomplished by shot-peening.
5. An elongated composite cladding tube for containing nuclear fuel as a fuel element for a nuclear reactor, said composite cladding tube comprising a zirconium alloy tube containing constituents other than zirconium in an amount greater than 5000 parts per million and having a layer of zirconium metal containing impurities of less than 500 parts per million metallurgically bonded to the inside surface thereof, said zirconium metal layer being substantially fully recrystallized to provide a fine-grained microstructure therein, and said zirconium alloy tube being substantially full stress-relieved but not fully recrystallized.
6. A composite cladding tube as claimed in claim 5 wherein the surface of said zirconium metal layer is compressively deformed.
7. A composite cladding tube as claimed in claim 6 wherein said deforming is accomplished by shot-peening.
8. A method of making an elongated composite cladding tube for containing nuclear fuel as a fuel element for a nuclear reactor as claimed in claim 1 substantially as hereinbefore described with reference to and as illustrated in the accompanying drawings.
9. A method of making an elongated composition cladding tube for containing nuclear fuel as a fuel element for a nuclear reactor as claimed in claim 1 substantially as hereinbefore described in the Example.
10. A composite cladding tube when produced by a method as claimed in any one of claims 1 to 4 8 or 9.
11. A composite cladding tube as claimed in claim 5 substantially as hereinbefore described with reference to the accompnying drawings.
1 2. A composite cladding tube as claimed in claim 5 substantially as hereinbefore described in the Example.
GB8000027A 1979-06-04 1980-01-02 Nuclear fuel element cladding Expired GB2050206B (en)

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US4522579A 1979-06-04 1979-06-04

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GB2050206B GB2050206B (en) 1982-11-10

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BE (1) BE881341A (en)
CA (1) CA1139023A (en)
CH (1) CH644709A5 (en)
DE (1) DE3003610C2 (en)
ES (2) ES8207643A1 (en)
FR (1) FR2458876A1 (en)
GB (1) GB2050206B (en)
IT (1) IT1129692B (en)
MX (1) MX6773E (en)
SE (2) SE436047B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0071193A1 (en) * 1981-07-29 1983-02-09 Hitachi, Ltd. Process for producing zirconium-based alloy
GB2119559A (en) * 1982-05-03 1983-11-16 Gen Electric Zirconium alloy barrier having improved corrosion resistance
GB2172737A (en) * 1985-03-19 1986-09-24 Cezus Co Europ Zirconium Composite sheath tubes for nuclear fuel and their production
GB2179876A (en) * 1985-06-25 1987-03-18 Wiederaufarbeitung Von Kernbre Coating a hollow body
EP0634752A1 (en) * 1993-07-14 1995-01-18 General Electric Company Method for making fuel cladding having zirconium barrier layers
US5517541A (en) * 1993-07-14 1996-05-14 General Electric Company Inner liners for fuel cladding having zirconium barriers layers

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE426890B (en) * 1981-07-07 1983-02-14 Asea Atom Ab SET TO MANUFACTURE Capsules of Zirconium-Based Alloy for Fuel Rods for Nuclear Reactors
SE426891B (en) * 1981-07-07 1983-02-14 Asea Atom Ab SET TO MANUFACTURE Capsules of Zirconium-Based Alloy COMBUSTION RODS FOR NUCLEAR REACTORS
GB2104711B (en) * 1981-08-24 1985-05-09 Gen Electric Nuclear fuel element and method of producing same
US4770847A (en) * 1982-06-01 1988-09-13 General Electric Company Control of differential growth in nuclear reactor components by control of metallurgical conditions
DE3248686A1 (en) * 1982-12-30 1984-07-12 Kraftwerk Union AG, 4330 Mülheim METHOD FOR PRODUCING A SUCTION TUBE FROM A ZIRCONIUM ALLOY FOR CORE REACTOR FUEL OF A CORE REACTOR FUEL ELEMENT
JPS60165580A (en) * 1984-02-08 1985-08-28 株式会社日立製作所 Coated tube for reactor fuel and manufacture thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3287111A (en) * 1965-10-14 1966-11-22 Harold H Klepfer Zirconium base nuclear reactor alloy
CA1025335A (en) * 1972-09-05 1978-01-31 Ake S.B. Hofvenstam Method of making tubes and similar products of a zirconium alloy
GB1528142A (en) * 1974-11-11 1978-10-11 Gen Electric Nuclear fuel elements
GB1525717A (en) * 1974-11-11 1978-09-20 Gen Electric Nuclear fuel elements
FR2404898B2 (en) * 1974-11-11 1986-05-02 Gen Electric COMPOSITE SHEATH FOR A NUCLEAR FUEL ELEMENT
FR2334763A1 (en) * 1975-12-12 1977-07-08 Ugine Aciers PROCESS FOR IMPROVING THE HOT RESISTANCE OF ZIRCONIUM AND ITS ALLOYS
JPS5332298A (en) * 1976-09-06 1978-03-27 Toshiba Corp Fuel element
GB1569078A (en) * 1977-09-30 1980-06-11 Gen Electric Nuclear fuel element

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0071193A1 (en) * 1981-07-29 1983-02-09 Hitachi, Ltd. Process for producing zirconium-based alloy
GB2119559A (en) * 1982-05-03 1983-11-16 Gen Electric Zirconium alloy barrier having improved corrosion resistance
GB2172737A (en) * 1985-03-19 1986-09-24 Cezus Co Europ Zirconium Composite sheath tubes for nuclear fuel and their production
GB2179876A (en) * 1985-06-25 1987-03-18 Wiederaufarbeitung Von Kernbre Coating a hollow body
EP0634752A1 (en) * 1993-07-14 1995-01-18 General Electric Company Method for making fuel cladding having zirconium barrier layers
US5517541A (en) * 1993-07-14 1996-05-14 General Electric Company Inner liners for fuel cladding having zirconium barriers layers

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BE881341A (en) 1980-05-16
SE8000838L (en) 1980-12-05
ES494204A0 (en) 1982-11-01
JPS62272188A (en) 1987-11-26
ES487846A0 (en) 1982-09-16
ES8207643A1 (en) 1982-09-16
CA1139023A (en) 1983-01-04
FR2458876A1 (en) 1981-01-02
IT1129692B (en) 1986-06-11
SE9402593D0 (en) 1994-07-28
MX6773E (en) 1986-07-08
JPS6313160B2 (en) 1988-03-24
DE3003610C2 (en) 1986-07-10
SE436047B (en) 1984-11-05
JPS6055036B2 (en) 1985-12-03
JPS55164396A (en) 1980-12-22
ES8301046A1 (en) 1982-11-01
GB2050206B (en) 1982-11-10
DE3003610A1 (en) 1980-12-11
IT8019592A0 (en) 1980-01-31
FR2458876B1 (en) 1983-12-16
CH644709A5 (en) 1984-08-15

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Effective date: 19970102