EP0248396A2 - Procédé pour la fabrication de matériaux de gainage par une combinaison d'une fusion par un faisceau d'électrons et par arc sous vide - Google Patents
Procédé pour la fabrication de matériaux de gainage par une combinaison d'une fusion par un faisceau d'électrons et par arc sous vide Download PDFInfo
- Publication number
- EP0248396A2 EP0248396A2 EP87107945A EP87107945A EP0248396A2 EP 0248396 A2 EP0248396 A2 EP 0248396A2 EP 87107945 A EP87107945 A EP 87107945A EP 87107945 A EP87107945 A EP 87107945A EP 0248396 A2 EP0248396 A2 EP 0248396A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- melting
- ingot
- process according
- zirconium
- sponge
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000002844 melting Methods 0.000 title claims abstract description 34
- 230000008018 melting Effects 0.000 title claims abstract description 34
- 238000010894 electron beam technology Methods 0.000 title claims abstract description 33
- 230000004888 barrier function Effects 0.000 title 1
- 239000011257 shell material Substances 0.000 title 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 16
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 16
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 8
- 229910052786 argon Inorganic materials 0.000 claims description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 4
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- 229910052735 hafnium Inorganic materials 0.000 description 7
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229910001093 Zr alloy Inorganic materials 0.000 description 6
- 239000012535 impurity Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000005253 cladding Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 239000003758 nuclear fuel Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- OOAWCECZEHPMBX-UHFFFAOYSA-N oxygen(2-);uranium(4+) Chemical compound [O-2].[O-2].[U+4] OOAWCECZEHPMBX-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007514 turning Methods 0.000 description 1
- FCTBKIHDJGHPPO-UHFFFAOYSA-N uranium dioxide Inorganic materials O=[U]=O FCTBKIHDJGHPPO-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
- C22B9/16—Remelting metals
- C22B9/20—Arc remelting
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B34/00—Obtaining refractory metals
- C22B34/10—Obtaining titanium, zirconium or hafnium
- C22B34/14—Obtaining zirconium or hafnium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
- C22B9/16—Remelting metals
- C22B9/22—Remelting metals with heating by wave energy or particle radiation
- C22B9/228—Remelting metals with heating by wave energy or particle radiation by particle radiation, e.g. electron beams
Definitions
- This invention relates to the production of purified zirconium.
- the conventional process for making zirconium metal utilizes a fluidized bed process in which the ore is subjected to a chlorination step which produces a relatively impure, hafnium-containing zirconium tetrachloride and by-product silicon tetrachloride (which by-product is relatively easily separated).
- the hafnium and zirconium containing material is then subjected to a number of purifying operations and also a complex hafnium separation operation. These operations result in purified oxides of zirconium and hafnium, which, of course, are maintained separate.
- the purified oxides are separately chlorinated.
- Zirconium and hafnium are commonly reduced from the chloride by means of a reducing metal, typically magnesium.
- a reducing metal typically magnesium.
- the commercial processes are batched-type processes.
- U.S. Patent Specification No. 3,966,460 describes a process of introducing zirconium tetrachloride vapor onto molten magnesium, with the zirconium being reduced and traveling down through the magnesium layer to the bottom of the reactor and forming a metallic sponge.
- the metalic sponge (containing remaining chloride and some remaining excess reducing metal) is then placed in a distillation vessel for removal of the remaining salt and reducing metal by high temperature vacuum distillation.
- the sponge material is generally crushed, screened and pressed into electrodes for vacuum arc melting. Particularly, the material is multiple (typical double or triple) vacuum arc melted to provide ingots which are then further fabricated into various shapes.
- Most of the zirconium currently is used to produce Zircaloy.
- Zircaloy tubes as cladding material to contain the uranium dioxide fuel.
- a Zircaloy ingot is processed into a so-called "trex" and pilgering operations are used to reduce the trex inside diameter and wall thickness to size.
- Ultra-pure zirconium has been proposed for a liner for the inside surface of Zircaloy tubing which is used as a cladding for nuclear fuel and is described in, for example, U.S. Patent Specification No. 4,372,817 (Armijo et al.).
- a similar use of moderate purity material is proposed in U.S. Patent Specification No. 4,200,492 (Armijo et al.).
- EB (electron beam) melting of materials has been discussed in a number of U.S. patent specifications.
- EB melting has been used to consolidate crushed particles or chips in so called hearth furnaces and to separate impurities by either overflowing floating inclusions (U.S. Patent Specification No. 4,190,404 (Drs et al.)) or to produce an electrode for arc melting (U.S. Patent Specification No. 4,108,644 (Walberg et al.)).
- U.S. patent specifications have described the EB melting of powders or granules, often producing an ingot in a chilled mold. These powder melting EB patents include U.S. Patent Specification No.
- U.S. Patent Specification No. 3,091,525 (D'A. Hunt) describes adding a small amount of zirconium, for example, to hafnium, for example and melting in an EB furnace to deoxidize the hafnium.
- Japanese application 1979-144789 Kawakita published as patent publication 1981-67788 describes the use of a very small ingot with a high power density and ultra slow melting to produce a deep molten pool to produce a high purity ingot directly usable for lining of Zircaloy tubing for nuclear reactor applications.
- Such laboratory sized apparatus with its high powered consumption and very low throughput is, of course, not practical for commercial production.
- a process for producing zirconium in purified form comprises reducing zirconium tetrachloride to produce a sponge of metallic zirconium which is distilled to generally remove residual magnesium and magnesium chloride, and melting the distilled sponge to produce an ingot, characterized by forming said distilled sponge into a consumable electrode; melting said consumable electrode in a multiple swept beam electron furnace with a feed rate of from 1 to 20 inches per hour to form an intermediate ingot; and vacuum arc melting said intermediate ingot to produce a final ingot.
- this process provides material much purer than the so called sponge material and almost as pure as the crystal bar material, at a fraction of the cost of crystal bar material.
- Generally purified zirconium produced according to the present invention has oxygen in the 250-450 ppm range (and preferably less than about 350) and iron in the 50-300 ppm range.
- Total impurities are generally in the 500-1000 ppm range (total impurities for these purposes generally comprise the elements listed in the afore-mentioned U.S. Patent Specification No. 4,200,492).
- the energy input via the electron beams is maintained to a moderate level such that the molten pool on the upper portion of the intermediate ingot has a depth of less than about one fourth of the ingot diameter, thus lowering power costs.
- an argon sweep is provided in the electron beam furnace during melting. Multiple passes may be made both through the EB furnace and the vacuum arc furnace.
- the distilled zirconium sponge is formed into a consumable electrode for use in a production EB furnace.
- a production furnace is generally shown in the afore-mentioned U.S. Patent Specification No. 3,219,435, but with the multiple beams being constantly swept across the surface of the molten pool (as defined herein, a production EB furnace has an output "intermediate" ingot having a diameter greater than five inches, and generally greater than six inches.
- this consumable electrode for EB melting is formed by pressing crushed virgin sponge (not recycle scrap). The compact and an appropriate end fitting are welded to form the consumable electrode.
- the consumable EB electrode is melted in a production electron beam furnace with a feed rate of from 1 to 20 inches per hour. It has been found that small amounts of residual magnesium chloride remain in the electrode and absorb some moisture. Melting at faster than 20 inches per hour results in this moisture reacting to oxidized zirconium and thus causing an unacceptably high oxygen level in the product. Conversely too slow a melting rate, while possibly removing some oxygen from the molten pool (as described in the afore-mentioned Japanese patent publication 1981-67788) is uneconomical. It should be noted that significant oxygen removal from the molten pool takes considerable superheating of the molten pool and much slower melting rates and thus this invention provides for no significant oxygen removal from the molten pool.
- the iron impurity level is generally reduced by about a factor of two, each pass through the EB furnace (that is, when the intermediate ingot formed during the first EB melting pass is used as the consumable electrode for a second EB melting, the iron level is reduced by another factor of approximately 2). It has also been found that the level of other common impurities, for example aluminum and chromium, are also reduced by each pass through the EB furnace. It should also be noted that, as the residual magnesium chloride is generally removed during the first EB melting, there is minimal absorbed moisture on the second pass and thus somewhat faster speeds may be used after the first EB pass.
- an argon sweep is provided in the electron beam furnace during melting. It is felt that this helps remove moisture which has been vaporized off the electron from the furnace, minimizing contamination of the output intermediate ingot.
- the argon sweep is at a flow of 10,000-1,000,000 liters per second, with the liters measured at a pressure of 10 ⁇ 5 Torr (rather than at standard conditions).
- the argon sweep can be established, for example, with pumps capable of handling 60,000 liters per second and with a pressure of 10 ⁇ 5 Torr measured with no argon flow, by controlling argon introduction to a rate to raise the pressure to approximately 10 ⁇ 4 Torr.
- the sponge used to form the consumable electrode is generally virgin material (as opposed to recycled scrap or turnings) and preferably is selected high quality material and generally selected for low oxygen content.
- the material is arc melted (and preferably double arc melted or even triple arc melted) to homogenize the impurity distribution. It has been found that in production EB furnaces, with their relatively shallow molten pool (the molten pool being shallow both in comparison to arc melting, where the molten pool is typically about twice the ingot diameter and in comparison to non-multiple swept beam, laboratory type furnaces where the fixed single beam covers essentially the entire surface of the molten pool and produces molten pools of about one diameter in depth) do not produce a homogeneous product.
- the zirconium material beneath the molten pool is, of course, solid, and can be slowly withdrawn as material from the electrode drips into the pool, as it is known in the prior art.
- the shallow molten pool results in a non-homogeneous product, and only by following such melting with vacuum arc melting can a homogeneous product be obtained.
- non-swept beam EB furnaces having very high power costs for very low throughput, are impractical for commercial applications.
- This invention lowers oxygen by removing at least some of the moisture prior to melting while the laboratory type of EB furnace is generally removing oxygen from the molten pool.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Manufacture And Refinement Of Metals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87118386A | 1986-06-05 | 1986-06-05 | |
US871183 | 1986-06-05 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0248396A2 true EP0248396A2 (fr) | 1987-12-09 |
EP0248396A3 EP0248396A3 (en) | 1990-04-25 |
EP0248396B1 EP0248396B1 (fr) | 1993-04-28 |
Family
ID=25356891
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87107945A Expired - Lifetime EP0248396B1 (fr) | 1986-06-05 | 1987-06-02 | Procédé pour la fabrication de matériaux de gainage par une combinaison d'une fusion par un faisceau d'électrons et par arc sous vide |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0248396B1 (fr) |
KR (1) | KR880000607A (fr) |
DE (1) | DE3785605T2 (fr) |
ES (1) | ES2040712T3 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0320730A2 (fr) * | 1987-12-18 | 1989-06-21 | Westinghouse Electric Corporation | Procédé pour produire du zirconium pour des gaines de combustible nucléaire |
US5062887A (en) * | 1991-02-08 | 1991-11-05 | Westinghouse Electric Corp. | Process for chloride removal from sponge metal |
US6036741A (en) * | 1997-07-31 | 2000-03-14 | Japan Energy Corporation | Process for producing high-purity ruthenium |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1121281B (de) * | 1959-11-07 | 1962-01-04 | Heraeus Gmbh W C | Schmelzanlage zum Schmelzen von Metallen unter reduziertem Druck |
US3091525A (en) * | 1959-05-01 | 1963-05-28 | Stauffer Chemical Co | Deoxidation of refractory metal |
FR1331472A (fr) * | 1962-05-22 | 1963-07-05 | Applic Electro Thermiques Et C | Procédé pour la purification de métaux à température de fusion élevée, notamment du zirconium, et dispositif pour la mise en oeuvre de ce procédé |
US3219435A (en) * | 1959-04-24 | 1965-11-23 | Heraeus Gmbh W C | Method and apparatus for producing metal blocks by electron beams |
US4108644A (en) * | 1976-11-11 | 1978-08-22 | Viking Metallurgical Corp. | Manufacture of reactive metals and alloys |
JPS5667788A (en) * | 1979-11-08 | 1981-06-08 | Tokyo Shibaura Electric Co | Manufacture of cladding tube for nuclear fuel element |
EP0146314A2 (fr) * | 1983-12-07 | 1985-06-26 | Hitachi, Ltd. | Méthode de production d'une piéce métallique de haute pureté |
-
1987
- 1987-06-02 ES ES198787107945T patent/ES2040712T3/es not_active Expired - Lifetime
- 1987-06-02 EP EP87107945A patent/EP0248396B1/fr not_active Expired - Lifetime
- 1987-06-02 DE DE8787107945T patent/DE3785605T2/de not_active Expired - Fee Related
- 1987-06-05 KR KR870005720A patent/KR880000607A/ko not_active Application Discontinuation
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3219435A (en) * | 1959-04-24 | 1965-11-23 | Heraeus Gmbh W C | Method and apparatus for producing metal blocks by electron beams |
US3091525A (en) * | 1959-05-01 | 1963-05-28 | Stauffer Chemical Co | Deoxidation of refractory metal |
DE1121281B (de) * | 1959-11-07 | 1962-01-04 | Heraeus Gmbh W C | Schmelzanlage zum Schmelzen von Metallen unter reduziertem Druck |
FR1331472A (fr) * | 1962-05-22 | 1963-07-05 | Applic Electro Thermiques Et C | Procédé pour la purification de métaux à température de fusion élevée, notamment du zirconium, et dispositif pour la mise en oeuvre de ce procédé |
US4108644A (en) * | 1976-11-11 | 1978-08-22 | Viking Metallurgical Corp. | Manufacture of reactive metals and alloys |
JPS5667788A (en) * | 1979-11-08 | 1981-06-08 | Tokyo Shibaura Electric Co | Manufacture of cladding tube for nuclear fuel element |
EP0146314A2 (fr) * | 1983-12-07 | 1985-06-26 | Hitachi, Ltd. | Méthode de production d'une piéce métallique de haute pureté |
Non-Patent Citations (2)
Title |
---|
Winkler et al., VACUUM METALLURGY, 1971, Elsevier, Amsterdam-London-New York; pp. 270, 271, 618, 619, 625, 626# * |
WINKLER et al.: VACUUM METALLURGY * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0320730A2 (fr) * | 1987-12-18 | 1989-06-21 | Westinghouse Electric Corporation | Procédé pour produire du zirconium pour des gaines de combustible nucléaire |
EP0320730A3 (fr) * | 1987-12-18 | 1990-02-14 | Westinghouse Electric Corporation | Procédé pour produire du zirconium pour des gaines de combustible nucléaire |
US5062887A (en) * | 1991-02-08 | 1991-11-05 | Westinghouse Electric Corp. | Process for chloride removal from sponge metal |
US6036741A (en) * | 1997-07-31 | 2000-03-14 | Japan Energy Corporation | Process for producing high-purity ruthenium |
Also Published As
Publication number | Publication date |
---|---|
DE3785605D1 (de) | 1993-06-03 |
EP0248396A3 (en) | 1990-04-25 |
KR880000607A (ko) | 1988-03-28 |
EP0248396B1 (fr) | 1993-04-28 |
ES2040712T3 (es) | 1993-11-01 |
DE3785605T2 (de) | 1993-08-12 |
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