US2938841A - Preparation of zirconium for cold working - Google Patents
Preparation of zirconium for cold working Download PDFInfo
- Publication number
- US2938841A US2938841A US577921A US57792156A US2938841A US 2938841 A US2938841 A US 2938841A US 577921 A US577921 A US 577921A US 57792156 A US57792156 A US 57792156A US 2938841 A US2938841 A US 2938841A
- Authority
- US
- United States
- Prior art keywords
- zirconium
- per liter
- coating
- zinc
- copper
- 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.)
- Expired - Lifetime
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- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 title claims description 75
- 229910052726 zirconium Inorganic materials 0.000 title claims description 75
- 238000005482 strain hardening Methods 0.000 title claims description 20
- 238000002360 preparation method Methods 0.000 title description 2
- 238000000576 coating method Methods 0.000 claims description 52
- 239000011248 coating agent Substances 0.000 claims description 49
- 229910052751 metal Inorganic materials 0.000 claims description 35
- 239000002184 metal Substances 0.000 claims description 35
- 239000000243 solution Substances 0.000 claims description 34
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 30
- 239000011701 zinc Substances 0.000 claims description 23
- 229910052725 zinc Inorganic materials 0.000 claims description 23
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 22
- 239000007864 aqueous solution Substances 0.000 claims description 14
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 10
- 238000000151 deposition Methods 0.000 claims description 7
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 claims description 7
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 claims description 7
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 7
- 229910000368 zinc sulfate Inorganic materials 0.000 claims description 7
- 229960001763 zinc sulfate Drugs 0.000 claims description 7
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 6
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- RCIVOBGSMSSVTR-UHFFFAOYSA-L stannous sulfate Chemical compound [SnH2+2].[O-]S([O-])(=O)=O RCIVOBGSMSSVTR-UHFFFAOYSA-L 0.000 claims description 4
- 229910000375 tin(II) sulfate Inorganic materials 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 38
- 229910052802 copper Inorganic materials 0.000 description 38
- 239000010949 copper Substances 0.000 description 38
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 25
- 239000011135 tin Substances 0.000 description 24
- 229910052718 tin Inorganic materials 0.000 description 24
- 238000000034 method Methods 0.000 description 22
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 229960002050 hydrofluoric acid Drugs 0.000 description 12
- 239000010408 film Substances 0.000 description 11
- -1 fluoride ions Chemical class 0.000 description 10
- 229910001369 Brass Inorganic materials 0.000 description 7
- 239000010951 brass Substances 0.000 description 7
- 238000009713 electroplating Methods 0.000 description 7
- 238000007747 plating Methods 0.000 description 7
- 238000006722 reduction reaction Methods 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 230000001464 adherent effect Effects 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 238000000137 annealing Methods 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 229960002163 hydrogen peroxide Drugs 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 229910001432 tin ion Inorganic materials 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- 230000003245 working effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241000080590 Niso Species 0.000 description 2
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
- MIMUSZHMZBJBPO-UHFFFAOYSA-N 6-methoxy-8-nitroquinoline Chemical compound N1=CC=CC2=CC(OC)=CC([N+]([O-])=O)=C21 MIMUSZHMZBJBPO-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001208007 Procas Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- LEKPFOXEZRZPGW-UHFFFAOYSA-N copper;dicyanide Chemical compound [Cu+2].N#[C-].N#[C-] LEKPFOXEZRZPGW-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 238000005323 electroforming Methods 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229940099596 manganese sulfate Drugs 0.000 description 1
- 239000011702 manganese sulphate Substances 0.000 description 1
- 235000007079 manganese sulphate Nutrition 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- VBKNTGMWIPUCRF-UHFFFAOYSA-M potassium;fluoride;hydrofluoride Chemical compound F.[F-].[K+] VBKNTGMWIPUCRF-UHFFFAOYSA-M 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/34—Pretreatment of metallic surfaces to be electroplated
- C25D5/38—Pretreatment of metallic surfaces to be electroplated of refractory metals or nickel
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/934—Electrical process
- Y10S428/935—Electroplating
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12708—Sn-base component
- Y10T428/12715—Next to Group IB metal-base component
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12708—Sn-base component
- Y10T428/12722—Next to Group VIII metal-base component
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12785—Group IIB metal-base component
- Y10T428/12792—Zn-base component
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12785—Group IIB metal-base component
- Y10T428/12792—Zn-base component
- Y10T428/12799—Next to Fe-base component [e.g., galvanized]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12806—Refractory [Group IVB, VB, or VIB] metal-base component
Definitions
- This invention relates generally to metal treating and more particularly to zirconium and to methods for placing a metallic coating thereon and to a process for cold working zirconium.
- Zirconium because of its low neutron absorption, is particularly advantageous for making containers and other metallic parts to be used in conjunction with atomic engines and for the transportation of radioactive material.
- a layer of an adherent abrasive scale is formed on zirconium when it is exposed to the air and zirconium has a rapid Work hardening rate. Consequently, it is extremely diificult to cold work the metal and a special treatment is required before it can be elongated without fracturing by cold rolling, deep drawing, extruding and similar cold Working processes.
- One method for removing the scale from zirconium available heretofore involves removing the scale by abrasive polishing, such as wire brushing and grit blasting.
- the freshly brushed surface is deeply etched in a chemical solution and coated with a layer of nickel by an electroplating process.
- the plated metal must next be hardened to bring about diffusion and alloying of the nickel with the zirconium.
- Such a process is laborious, requires the use of specialized expensive equipment and, in order to recover a zirconium surface, the alloy must be machined from the surface.
- Zirconium has the additional undesirable characteristic of readily reacting with hydrogen, nitrogen and oxygen when heated and as a result it has been necessary heretofore to anneal the zirconium in vacuo'.
- an object of this invention to provide an improved method for cold working zirconium.
- Another object of this invention is to provide a process for preparing zirconium for cold working.
- a further object of the invention is to provide a method for placing on zirconium a protective coating of another metal.
- a still further object of this invention is to provide a method for annealing zirconium in air; i.e., without evacuating the annealing furnace.
- Still another object of the invention is to provide a solution and process for removing scale from the surface of zirconium.
- a still further object of the invention is to provide a solution for coating zirconium with a ductile metal.
- Another object of the inventio'n is to provide a process for lubricating zirconium while cold working.
- Another object of the invention is to provide a means for coating zirconium articles with an adherent and smooth deposit of a ductile material adapted to be removed by chemical means without etching the surface of the zirconium article.
- the scale is removed from the zirconium by immersing the zirconium article in an aqueous solution of nickel sulfate, fluoride ions and an oxidizing agent such as hydrogen peroxide.
- the cleaning is improved by including a minor amount of a wetting agent in the solution.
- the cleaned zirconium surface is first coated by chemical reduction with a layer of tin or zinc by immersing it in an aqueous solution of a soluble zinc or tin salt and fluoride ions and leaving it therein until the zinc or tin is deposited in a smooth adherent film on the zirconium. It has been found that zirconium coated with either tin or zinc has improved cold working properties over uncoated zirconium and that in some instances the cold working characteristics of zirconium may be further improved by coating the tin or zinc coating zirco'nium with another ductile metal.
- the tin or zinc coated zirconium is first coated with a very thin film of copper.
- a film of copper is commonly known in the industry as a copper strike.
- the copper surface may then be coated with a ductile metal by electroplating it in a suitable bath for electroplating copper with copper or for plating copper with any other ductile metal such as brass, iron, tin, lead and the like or by means of a suitable chemical reduction process.
- a more adherent coating is obtained when a copper strike is used even if the final coating is to be copper.
- a preferred solution from which copper may be electrolytically deposited over the copper strike is an alkaline cyanide copper solution. This solution may be used also for placing the copper strike on the article.
- the total thickness of the coating or coatings of metal on zirconium must be within the range of from about 0.001 inch to about 0.002 inch for satisfactory cold working. If the thickness is greater than this, the coating peels from the metal during the cold working operation and the zirconium is not properly protected if the thickness is less than 0.0008 inch.
- the scale appearing on the surface of metallic zirconium after exposure to the atmos-' phere may be removed rapidly without etching the metal by immersing the zirconium in an aqueous solution of from about 300 grams to about 700 grams of nickel sulfate (NiSO -7H O) per liter and fluoride ions in a concentration equivalent to from about 15 milliliters to about 30 milliliters of 48% hydrofluoric acid per liter at a temperature of from about 200 F. to about 210 F. Fifteen to thirty milliliters of hydrofluoric acid contain from about 7.75 grams to about 15.5 grams fluoride ions.
- NiSO -7H O nickel sulfate
- fluoride ions in a concentration equivalent to from about 15 milliliters to about 30 milliliters of 48% hydrofluoric acid per liter at a temperature of from about 200 F. to about 210 F.
- Fifteen to thirty milliliters of hydrofluoric acid contain from about 7.75 grams
- Zirconium may be coated with zinc by immersing it in an aqueous solution of from about 800 grams to about 1600 grams per liter zinc sulfate (ZnSO -7H 0), about 15 milliliters to about 30 milliliters 48% hydrofluoric acid (0.516 gram fluoride ion per milliliter) and from about 15 grams to' about 30 grams per liter aluminum sulfate (Al SO Zinc is deposited upon the zirconium by chemical reduction in such a solution. Any suitable zinc salt may be substituted for zinc sulfate, such as, for example, zinc chloride, but the amount of zinc ion utilized in the solution should be substantially equivalent to the zinc ion concentration of the solution specified above.
- the fluoride ion may be supplied to the solution used to remove the scale from the zirconium and to the zinc coating solution by dissolving therein sodium fluoride, ammonium fluoride, ammonium bifluoride, potassium fluoride or potassium bifluoride or any other suitable fluoride salt provided the amount thereof is within the fluoride ion concentration obtained by the use of the above amounts of hydrofluoric acid.
- the plating solution will deposit a suitable coating of zinc on a properly cleaned zirconium surface by chemical reduction in from one-half to'- one minute while the solution is at room temperature, or inother words, within the neighborhood of about 20 C.-
- a suitable coating of tin may be applied to the properly cleaned zirconium article by immersing it in an aqueous solution of a salt and fluoride ions.
- a preterred ing from immersion in such a solution has been found particularly well suited for lubricating zirconium in cold workingoperations so thezirconium may be provided with a coating of from about 0.001 inch to about 0.002 inch tin and cold worked without any other coating of ductile metal. In some instances, it may be necessary to immerse the article longer than 10 minutes in order to obtain a coating of about .002 inch. If the metal is to be annealed, however, it is advisable to place a coating of copper or brass as described in more detail hereinafter over the tin.
- the tin coating may be from about 0.0005 to about 0.001 inch in thickness. Furthermore, if the amount of reduction in thickness of the metal during cold working is relatively great the added protection of the copper, brass, or the like over the tin is sometimes desirable.
- An aqueous solution found particularly well suited for placing, a thin film of copper over a zinc or tin coating on zirconium contains about 165 grams per liter copper cyanide, about 195 grams per liter sodium cyanide, about l20'grams per liter sodium carbonate and about 10 grams Rochelle salt.
- the solution should be at atemperature of between about 120 F. and about 140 F. and the article should be. electroplated for about two minutes at a current density of about 24 amperes per square foot after which time the current should be turned ofi. Thecurrent should then be turned on and the article plated for. about 5 minutes at about 12 amperes per square foot, to complete the copper strike.
- the film of copper obtained is about 0.00001 inch to about 0.00002 inch. If no other metal is to be placed on the copper, the thickness of the copper may be increased until the total thickness of the base coating of tin or Zinc, the copper strike and the final copper plate is about 0.002 inch by continuing the plating treatment.
- zirconium having a thin copper strike coating may be plated with a thicker coating of a ductile material such as, for example, copper, brass, tin, iron or the like in order to further improve the zirconium cold working characteristics.
- a ductile material such as, for example, copper, brass, tin, iron or the like
- Any suitable electroplating solution for plating over copper may be utilized for this purpose;
- the coating of these metals should be from about 0.0005to about 0.0010 inch or of suflicient thiCk-.
- the total thickness of the coating on the zirconiuni is within the range of about 0.001 to about 0.002 inch if the metal is to be cold worked such as by drawing or rolling.
- a solution suitable for placing a brass coating on copper has the following composition:
- a solution particularly well suited for immersion plating zirconium havinga film of tin or zinc and a film of copper thereon with iron has about the following composition:
- the cleaned zirconium article is coated with a layer of Zinc from about 0.0005 to about 0.001 inch thick by immersing it in a zinc plating solution having the composition specified hereinbefore at room temperature.
- - zinc plating solution is rinsed from the article with Water and a film of copper from about 0.00001 to about 0.00002 inch thickness is placed over the zinc by electroplating as described above After-the copper strike has been placed on the metal, the current islturned off the second time.
- the copper coated zirconium may then be coated with one'of the ductile metals until the total thickness of coatings on the zirconium is within the range of about 0.001 inch to about 0.002 inch.
- the zirconium is then coated with glycerine and' cylindrical blanks are cut therefrom and the blanks are drawn and shaped into a cup by conventional cold working methods with a punch and die.
- the coating adheres to the zirconium and elongates with it as it is cold worked and acts as a barrier between the cold working tools and the zirconium if its thickness is within the range specified above and the coating thus materially increases the life of the tools without scratching or otherwise marring the surface of the zirconium.
- zirconium cleaned and coated in accordance with this invention maybe heated to annealing temperatures without evacuating the annealing furnaces. Also annealing the coatedmetal is cleaned and pickled in a suitable aqueous solution and is then cold worked by rolling, drawing orsimilar process.
- the metallic coatingof tin or zincor the coating of one of these metals with another ductile metal such as iron, tin, copper and the like may be removed from the zirconium by immersi-ng the article'in a suitable solvent forthe coating which is not a solvent for thezirconium. After the coating has been removed, a bright zirconium finish is obtained without any etching or other marring of the surface.
- the process for preparing zirconium for cold working which comprises removing the oxide scale; in an aqueous solution of about 300 to about 700 grams nickel sulfate per liter, fluoride ions in a concentration equivalent to from about '15 to about 30 milliliters of 48 percent hydrofluoric acid per liter and hydro gen peroxide, coating the thus cleaned zirconium with a metal selected from the group consisting of tin and zinc by immersing it in an aqueous solution selected from the group consisting of solutions of tin ions at least equivalent to about 54 grams per liter of stannous sulfate with from about 15 to about 30 milliliters of 48% hydrofiuoric acid per liter and solutions of zinc ions containing from about 800 grams to about 1600 grams per liter of zinc sulfate (ZnSO -7H O), about 15 to 30 milliliters of 48% hydrofluoric acid per liter and from about 15 to about 30 grams per liter of aluminum sulfate, electrolytic
- the process for preparing zirconium for cold Working which comprises removing the oxide scale therefrom in an aqueous solution of from about 300 to about 700 grams nickel sulfate (NiSO -7H O) per liter, and from about 15 to about 30 milliliters of 48% hydrofluoric acid per liter at a temperature of from about 200 F.
- NiSO -7H O nickel sulfate
- the process for removing the oxide scale from zirconium which comprises immersing the zirconium in an aqueous solution consisting essentially of from 30 percent to 70 percent nickel sulfate, 1 percent to 3 percent hydrofluoric acid and minor amounts of hydrogen peroxide and a compatible wetting agent.
- a process for producing zirconium having an adherent, ductile electrodeposit of a metal on the surface thereof which comprises first depositing on the clean zirconium a coating of tin by chemical reduction in a solution consisting essentially of tin ions at least equivalent to about 54 grams per liter of stannous sulfate with from about to about 30 milliliters of 48 percent hydrofluoric 6 acid per liter, and thereafter coating the zirconium with a ductile metal.
- a solution for coating zirconium with zinc by chemical reduction which consists essentially of from 800 grams to 1600 grams per liter zinc sulfate (ZnSO -7H O) about 15 milliliters to about 30 milliliters 48 percent bydrofiuoric acid per liter, from about 15 grams to about 30 grams per liter aluminum sulfate (Al (SO 11.
- a method of coating zirconium articles with an adherent and smooth deposit of a ductile metal which comprises cleaning the zirconium article to remove substantially all of the surface oxide film, coating the cleaned article by immersing it in a solution selected from the group consisting of solutions of tin ions at least equivalent to about 54 grams per liter of stannous sulfate with from about 15 to about 30 milliliters of 48% hydrofiuoric acid per liter and solutions of zinc ions containing from about 800 grams to about 1600 grams per liter of zinc sulfate (ZnSO -7H O), about 15 to about 30 milliliters of 48% hydrofluoric acid per liter, and from about 15 to about 30 grams per liter of aluminum sulfate, and thereafter electrolytically depositing a coating of a ductile metal thereon.
- a process for improving the cold working properties of zirconium which comprises coating the zirconium with a film of ductile metal from about 0.001 to about 0.002 inch thick, said film being composed of a layer of tin adjacent the zirconium, a copper strike adjacent the tin, and an electrodeposited layer adjacent the copper strike of a ductile metal selected from the group consisting of copper, brass, tin, iron and lead.
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Description
PREPARATION OF ZIRCONIUM FOR COLD WORKING Kenneth H. Dale, Louisville, Ky., assignor to Olin Mathieson Chemical Corporation, East Alton, 11]., a corpora- No Drawing. Filed Apr. 13, 1956, Ser- No. 577,921
12 Claims. (Cl. 204-32) This invention relates generally to metal treating and more particularly to zirconium and to methods for placing a metallic coating thereon and to a process for cold working zirconium.
Zirconium, because of its low neutron absorption, is particularly advantageous for making containers and other metallic parts to be used in conjunction with atomic engines and for the transportation of radioactive material. A layer of an adherent abrasive scale is formed on zirconium when it is exposed to the air and zirconium has a rapid Work hardening rate. Consequently, it is extremely diificult to cold work the metal and a special treatment is required before it can be elongated without fracturing by cold rolling, deep drawing, extruding and similar cold Working processes. One method for removing the scale from zirconium available heretofore involves removing the scale by abrasive polishing, such as wire brushing and grit blasting. Then to improve thecold working properties of the metal, the freshly brushed surface is deeply etched in a chemical solution and coated with a layer of nickel by an electroplating process. The plated metal must next be hardened to bring about diffusion and alloying of the nickel with the zirconium. Such a process is laborious, requires the use of specialized expensive equipment and, in order to recover a zirconium surface, the alloy must be machined from the surface. Zirconium has the additional undesirable characteristic of readily reacting with hydrogen, nitrogen and oxygen when heated and as a result it has been necessary heretofore to anneal the zirconium in vacuo'.
It is, therefore, an object of this invention to provide an improved method for cold working zirconium. Another object of this invention is to provide a process for preparing zirconium for cold working. A further object of the invention is to provide a method for placing on zirconium a protective coating of another metal. A still further object of this invention is to provide a method for annealing zirconium in air; i.e., without evacuating the annealing furnace. Still another object of the invention is to provide a solution and process for removing scale from the surface of zirconium. A still further object of the invention is to provide a solution for coating zirconium with a ductile metal. Another object of the inventio'n is to provide a process for lubricating zirconium while cold working. Another object of the invention is to provide a means for coating zirconium articles with an adherent and smooth deposit of a ductile material adapted to be removed by chemical means without etching the surface of the zirconium article.
The foregoing objects as well as others are achieved in accordance with this invention, generally speaking, by providing a solution for removing the scale from zirconium by chemical means and a means for coating the cleaned zirconium surfaces with a coating of a ductile metal. In accordance with this invention, the scale is removed from the zirconium by immersing the zirconium article in an aqueous solution of nickel sulfate, fluoride ions and an oxidizing agent such as hydrogen peroxide.
nited States Patent C) 2,938,841 Patented May 31, 1960 lot:
The cleaning is improved by including a minor amount of a wetting agent in the solution. The cleaned zirconium surface is first coated by chemical reduction with a layer of tin or zinc by immersing it in an aqueous solution of a soluble zinc or tin salt and fluoride ions and leaving it therein until the zinc or tin is deposited in a smooth adherent film on the zirconium. It has been found that zirconium coated with either tin or zinc has improved cold working properties over uncoated zirconium and that in some instances the cold working characteristics of zirconium may be further improved by coating the tin or zinc coating zirco'nium with another ductile metal. When additional coatings are desired, the tin or zinc coated zirconium is first coated with a very thin film of copper. Such a film of copper is commonly known in the industry as a copper strike. The copper surface may then be coated with a ductile metal by electroplating it in a suitable bath for electroplating copper with copper or for plating copper with any other ductile metal such as brass, iron, tin, lead and the like or by means of a suitable chemical reduction process. A more adherent coating is obtained when a copper strike is used even if the final coating is to be copper. A preferred solution from which copper may be electrolytically deposited over the copper strike is an alkaline cyanide copper solution. This solution may be used also for placing the copper strike on the article.
The total thickness of the coating or coatings of metal on zirconium must be within the range of from about 0.001 inch to about 0.002 inch for satisfactory cold working. If the thickness is greater than this, the coating peels from the metal during the cold working operation and the zirconium is not properly protected if the thickness is less than 0.0008 inch.
It has been found that the scale appearing on the surface of metallic zirconium after exposure to the atmos-' phere may be removed rapidly without etching the metal by immersing the zirconium in an aqueous solution of from about 300 grams to about 700 grams of nickel sulfate (NiSO -7H O) per liter and fluoride ions in a concentration equivalent to from about 15 milliliters to about 30 milliliters of 48% hydrofluoric acid per liter at a temperature of from about 200 F. to about 210 F. Fifteen to thirty milliliters of hydrofluoric acid contain from about 7.75 grams to about 15.5 grams fluoride ions.
Zirconium may be coated with zinc by immersing it in an aqueous solution of from about 800 grams to about 1600 grams per liter zinc sulfate (ZnSO -7H 0), about 15 milliliters to about 30 milliliters 48% hydrofluoric acid (0.516 gram fluoride ion per milliliter) and from about 15 grams to' about 30 grams per liter aluminum sulfate (Al SO Zinc is deposited upon the zirconium by chemical reduction in such a solution. Any suitable zinc salt may be substituted for zinc sulfate, such as, for example, zinc chloride, but the amount of zinc ion utilized in the solution should be substantially equivalent to the zinc ion concentration of the solution specified above. The fluoride ion may be supplied to the solution used to remove the scale from the zirconium and to the zinc coating solution by dissolving therein sodium fluoride, ammonium fluoride, ammonium bifluoride, potassium fluoride or potassium bifluoride or any other suitable fluoride salt provided the amount thereof is within the fluoride ion concentration obtained by the use of the above amounts of hydrofluoric acid. The plating solution will deposit a suitable coating of zinc on a properly cleaned zirconium surface by chemical reduction in from one-half to'- one minute while the solution is at room temperature, or inother words, within the neighborhood of about 20 C.-
A suitable coating of tin may be applied to the properly cleaned zirconium article by immersing it in an aqueous solution of a salt and fluoride ions. A preterred ing from immersion in such a solution has been found particularly well suited for lubricating zirconium in cold workingoperations so thezirconium may be provided with a coating of from about 0.001 inch to about 0.002 inch tin and cold worked without any other coating of ductile metal. In some instances, it may be necessary to immerse the article longer than 10 minutes in order to obtain a coating of about .002 inch. If the metal is to be annealed, however, it is advisable to place a coating of copper or brass as described in more detail hereinafter over the tin. In'those instances where other metals are to be placed over the tin, the tin coating may be from about 0.0005 to about 0.001 inch in thickness. Furthermore, if the amount of reduction in thickness of the metal during cold working is relatively great the added protection of the copper, brass, or the like over the tin is sometimes desirable.
An aqueous solution found particularly well suited for placing, a thin film of copper over a zinc or tin coating on zirconium contains about 165 grams per liter copper cyanide, about 195 grams per liter sodium cyanide, about l20'grams per liter sodium carbonate and about 10 grams Rochelle salt. The solution should be at atemperature of between about 120 F. and about 140 F. and the article should be. electroplated for about two minutes at a current density of about 24 amperes per square foot after which time the current should be turned ofi. Thecurrent should then be turned on and the article plated for. about 5 minutes at about 12 amperes per square foot, to complete the copper strike. The film of copper obtained is about 0.00001 inch to about 0.00002 inch. If no other metal is to be placed on the copper, the thickness of the copper may be increased until the total thickness of the base coating of tin or Zinc, the copper strike and the final copper plate is about 0.002 inch by continuing the plating treatment.
As stated above, zirconium having a thin copper strike coating may be plated with a thicker coating of a ductile material such as, for example, copper, brass, tin, iron or the like in order to further improve the zirconium cold working characteristics. Any suitable electroplating solution for plating over copper may be utilized for this purpose; The coating of these metals should be from about 0.0005to about 0.0010 inch or of suflicient thiCk-.
ness that the total thickness of the coating on the zirconiuni is within the range of about 0.001 to about 0.002 inch if the metal is to be cold worked such as by drawing or rolling.
3 A solution suitable for placing a brass coating on copper has the following composition:
9 to 12 grams per liter zinc cyanide 19 to 25. grams per liter copper cyanide 12 to 16 grams per liter sodium carbonate 28 to 35 grams per liter sodium cyanite Temperature, 75 F.-100 F. v
Current density, 2.5-.-15 amperes per square foot Voltage, 1.5-2
A solution particularly well suited for immersion plating zirconium havinga film of tin or zinc and a film of copper thereon with iron has about the following composition:
Ferrous sulfate, FeSO -7H O 660 grams per liter. Hydrofluoric acid (48%) HF 230 milliliters per liter.
sulfate, Al (SO 5 grams per liter.
Manganese sulfate, MnSO grams per liter. Sodium alkyl aryl sulfonate .2 gram per liter. Temperature 150 F.
Time 5 to 10 minutes.
then rinsed in water at about 20 C. and is immediately immersed in a solution containing from about 300 to about 700 grams per liter nickel sulfate, 15 to milliliters per liter 48 percent hydrofluoricacid, 0.1 to 0.2 gram per liter sodium alkyl aryl sulfonate orother suitable wetting agent and about 0.5 to l milliliter per liter hydrogen peroxide at a temperatureof between about 200 F. and 210 F. until the scale on the surface of the zirconium has been removed.
The cleaned zirconium article is coated with a layer of Zinc from about 0.0005 to about 0.001 inch thick by immersing it in a zinc plating solution having the composition specified hereinbefore at room temperature. The
- zinc plating solution is rinsed from the article with Water and a film of copper from about 0.00001 to about 0.00002 inch thickness is placed over the zinc by electroplating as described above After-the copper strike has been placed on the metal, the current islturned off the second time. The copper coated zirconium may then be coated with one'of the ductile metals until the total thickness of coatings on the zirconium is within the range of about 0.001 inch to about 0.002 inch. The zirconium is then coated with glycerine and' cylindrical blanks are cut therefrom and the blanks are drawn and shaped into a cup by conventional cold working methods with a punch and die. It has been found that the coating adheres to the zirconium and elongates with it as it is cold worked and acts as a barrier between the cold working tools and the zirconium if its thickness is within the range specified above and the coating thus materially increases the life of the tools without scratching or otherwise marring the surface of the zirconium. p
As indicated hereinbefore zirconium cleaned and coated in accordance with this invention maybe heated to annealing temperatures without evacuating the annealing furnaces. Also annealing the coatedmetal is cleaned and pickled in a suitable aqueous solution and is then cold worked by rolling, drawing orsimilar process. The metallic coatingof tin or zincor the coating of one of these metals with another ductile metal such as iron, tin, copper and the like may be removed from the zirconium by immersi-ng the article'in a suitable solvent forthe coating which is not a solvent for thezirconium. After the coating has been removed, a bright zirconium finish is obtained without any etching or other marring of the surface. I Although the invention has been described in consider able detail in the foregoing, it is to be understood that such detail is solely for the purpose of clarifying the invention and that variations can be made therein by those skilled in the art without departing from the spirit and scope of the invention except as'it is limited by the appended claims. Iclaim: I V H l. The process for preparing zirconium for cold working which comprises removing the oxide scale; in an aqueous solution of about 300 to about 700 grams nickel sulfate per liter, fluoride ions in a concentration equivalent to from about '15 to about 30 milliliters of 48 percent hydrofluoric acid per liter and hydro gen peroxide, coating the thus cleaned zirconium with a metal selected from the group consisting of tin and zinc by immersing it in an aqueous solution selected from the group consisting of solutions of tin ions at least equivalent to about 54 grams per liter of stannous sulfate with from about 15 to about 30 milliliters of 48% hydrofiuoric acid per liter and solutions of zinc ions containing from about 800 grams to about 1600 grams per liter of zinc sulfate (ZnSO -7H O), about 15 to 30 milliliters of 48% hydrofluoric acid per liter and from about 15 to about 30 grams per liter of aluminum sulfate, electrolytically depositing a film of copper on the resulting surface, aud thereafter depositing a coating of a ductile metal over the copper film.
2. The process of claim 1 wherein the zirconium is plated with zinc after cleaning.
3. The process of claim 1 wherein the zirconium is plated with tin after cleaning.
4. The proca s of claim 1 wherein the final coating is copper.
5. The process of claim brass.
6. The process of claim 1 wherein the final coating is iron.
7. The process for preparing zirconium for cold Working which comprises removing the oxide scale therefrom in an aqueous solution of from about 300 to about 700 grams nickel sulfate (NiSO -7H O) per liter, and from about 15 to about 30 milliliters of 48% hydrofluoric acid per liter at a temperature of from about 200 F. to about 210 F, coating the zirconium with zinc by immersing it 1 wherein the final coating is in a solution of from about 800 to about 1600 grams per liter zinc sulfate (ZnSO -7H O), about 15 to about 30 milliliters 48% hydrofluoric acid per liter, from about 15 to about 30 grams per liter aluminum sulfate (Al (SO in an aqueous solution, depositing a coating of copper over the zinc by electroplating with a current density of at least about 15 amperes per square foot in a solution containing about 165 grams per liter copper cyanide, about 195 grams per liter sodium cyanide, about 120 grams per liter sodium carbonate and about 10 grams per liter Rochelle salt at a temperature of from about 120 F. to 140 F., and thereafter depositing a coating of a duotile metal over the copper strike.
8. The process for removing the oxide scale from zirconium which comprises immersing the zirconium in an aqueous solution consisting essentially of from 30 percent to 70 percent nickel sulfate, 1 percent to 3 percent hydrofluoric acid and minor amounts of hydrogen peroxide and a compatible wetting agent.
9. A process for producing zirconium having an adherent, ductile electrodeposit of a metal on the surface thereof which comprises first depositing on the clean zirconium a coating of tin by chemical reduction in a solution consisting essentially of tin ions at least equivalent to about 54 grams per liter of stannous sulfate with from about to about 30 milliliters of 48 percent hydrofluoric 6 acid per liter, and thereafter coating the zirconium with a ductile metal.
10. A solution for coating zirconium with zinc by chemical reduction which consists essentially of from 800 grams to 1600 grams per liter zinc sulfate (ZnSO -7H O) about 15 milliliters to about 30 milliliters 48 percent bydrofiuoric acid per liter, from about 15 grams to about 30 grams per liter aluminum sulfate (Al (SO 11. A method of coating zirconium articles with an adherent and smooth deposit of a ductile metal which comprises cleaning the zirconium article to remove substantially all of the surface oxide film, coating the cleaned article by immersing it in a solution selected from the group consisting of solutions of tin ions at least equivalent to about 54 grams per liter of stannous sulfate with from about 15 to about 30 milliliters of 48% hydrofiuoric acid per liter and solutions of zinc ions containing from about 800 grams to about 1600 grams per liter of zinc sulfate (ZnSO -7H O), about 15 to about 30 milliliters of 48% hydrofluoric acid per liter, and from about 15 to about 30 grams per liter of aluminum sulfate, and thereafter electrolytically depositing a coating of a ductile metal thereon.
12. A process for improving the cold working properties of zirconium which comprises coating the zirconium with a film of ductile metal from about 0.001 to about 0.002 inch thick, said film being composed of a layer of tin adjacent the zirconium, a copper strike adjacent the tin, and an electrodeposited layer adjacent the copper strike of a ductile metal selected from the group consisting of copper, brass, tin, iron and lead.
References Cited in the file of this patent UNITED STATES PATENTS 1,248,107 Hathaway Nov. 27, 1917 1,948,485 Anselm Feb. 27, 1934 2,370,973 Lang Mar. 6, 1945 2,496,845 Balden et a1. Feb. 7, 1950 2,564,549 Stargarter Aug. 14, 1951 2,580,773 Heiman Jan. 1, 1952 2,624,684 Heiman Jan. 6, 1953 2,646,396 Dean July 21, 1953 2,653,134 Dilling et a1 Sept. 22, 1953 2,711,389 Beach et a1 June 21, 1955 2,734,837 Hands Feb. 14, 1956 2,776,255 Hammond et a1. Jan. 1, 1957 2,798,843 Slomin et al July 9, 1957 2,801,213 Beuckman et al. July 30, 1957 2,825,682 Missel et a1 Mar. 4, 1958 2,835,630 Huddle et al May 20, 1958 OTHER REFERENCES Principles of Electroplating and Electroforming, Blum et 21.1., 3rd edition (1949), McGraw-Hill Book Company, Inc., New York, pages 379-381.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent Neg 2 9S8,84l May LII 1960 Kenneth Hc Dale It is hereby certified that error appears in the-printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Colman 2. line "coating" read coated column 4 Tine 7 for "container" read containing line 13 for "ofi'" read of same column 4 line 50 for "Also" read After Signed and sealed this 8th day of November 1960o (SEAL) Attest:
KARL AXLINE ROBERT C. WATSON Attesting Oflicer Commissioner of Patents
Claims (1)
1. THE PROCESS FOR PREPARING ZIRCONIUM FOR COLD WORKING WHICH COMPRISES REMOVING THE OXIDE SCALE IN AN AQUEOUS SOLUTION OF ABOUT 300 TO ABOUT 700 GRAMS NICKEL SULFATE PER LITER, FLUORIDE IONS IN A CONCENTRATION EQUIVALENT TO FROM ABOUT 15 TO ABOUT 30 MILLILITERS OF 48 PERCENT HYDROFLUORIC ACID PER LITER AND HYDROGEN PEROXIDE, COATING THE THUS CLEANED ZIRCONIUM WITH A METAL SELECTED FROM THE GROUP CONSISTING OF TIN AND ZINC BY IMMERSING IT IN AN AQUEOUS SOLUTION SELECTED FROM THE GROUP CONSISTING OF SOLUTIONS OF TIN IONS AT LEAST EQUIVALENT TO ABOUT 54 GRAMS PER LITER OF STANNOUS SULFATE WITH FROM ABOUT 15 TO ABOUT 30 MILLITERS OF 48% HYDROFLUORIC ACID PER LITER AND SOLUTIONS OF ZINC IONS CONTAINING FROM ABOUT 800 GRAMS TO ABOUT 1600 GRAMS PER LITER OF ZINC SULFATE (ZNSO4 7H2O), ABOUT 15 TO 30 MILLILITERS OF 48% HYDROFLUORIC ACID PER LITER AND FROM ABOUT 15 TO ABOUT 30 GRAMS PER LITER OF ALUMINUM SULFATE, ELECTROLYTICALLY DEPOSITISNG A FILM OF COPPER ON THE RESULTING SURFACE, AND THEREAFTER DEPOSITING A COATING OF A DUCTILE METAL OVER THE COPPER FILM.
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Cited By (7)
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US3202530A (en) * | 1961-11-30 | 1965-08-24 | Olin Mathieson | Method of forming a composite metal article |
US3328271A (en) * | 1964-09-22 | 1967-06-27 | Nat Res Corp | Method of electroplating copper on niobium-zirconium alloy superconductors for stabilization |
US3342648A (en) * | 1963-04-22 | 1967-09-19 | Westinghouse Electric Corp | Production of tubing |
US3368951A (en) * | 1964-02-17 | 1968-02-13 | Union Carbide Corp | Metal plating process and article made thereby |
US5264109A (en) * | 1991-09-16 | 1993-11-23 | Siemens Power Corporation | Zirconium and zirconium alloy passivation process |
US5558759A (en) * | 1994-07-26 | 1996-09-24 | Sargent Manufacturing Company | Metal finishing process |
US6656606B1 (en) | 2000-08-17 | 2003-12-02 | The Westaim Corporation | Electroplated aluminum parts and process of production |
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US6656606B1 (en) | 2000-08-17 | 2003-12-02 | The Westaim Corporation | Electroplated aluminum parts and process of production |
US6692630B2 (en) | 2000-08-17 | 2004-02-17 | The Westaim Corporation | Electroplated aluminum parts and process for production |
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