US2992135A - Reacted coating of titanium - Google Patents

Reacted coating of titanium Download PDF

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Publication number
US2992135A
US2992135A US694934A US69493457A US2992135A US 2992135 A US2992135 A US 2992135A US 694934 A US694934 A US 694934A US 69493457 A US69493457 A US 69493457A US 2992135 A US2992135 A US 2992135A
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titanium
aluminum
coating
bath
minutes
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US694934A
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Walter L Finlay
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Crucible Steel Company of America
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Crucible Steel Company of America
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21C—MANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES OR PROFILES, OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
    • B21C1/00—Manufacture of metal sheets, metal wire, metal rods, metal tubes by drawing
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/12—Aluminium or alloys based thereon
    • 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
    • Y10S29/00—Metal working
    • Y10S29/045—Titanium
    • 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
    • Y10S428/936—Chemical deposition, e.g. electroless plating
    • 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
    • Y10S428/939—Molten or fused coating
    • 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
    • Y10T29/00—Metal working
    • Y10T29/49—Method of mechanical manufacture
    • Y10T29/4998—Combined manufacture including applying or shaping of fluent material
    • Y10T29/49982—Coating
    • 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
    • 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.]
    • Y10T428/12736—Al-base component
    • Y10T428/12743—Next to refractory [Group IVB, VB, or VIB] 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
    • 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
    • Y10T428/12861—Group VIII or IB metal-base component
    • Y10T428/12903—Cu-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
    • Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
    • Y10T428/264—Up to 3 mils

Definitions

  • This invention relates to titanium and titanium base alloys, and contemplates materially enhancing the utility of these materials, particularly for high temperature service, by the use of coatings of other metals which bond themselves to the base metal by penetrating and alloying or combining therewith.
  • titanium and its alloys oifer a unique combination of high tensile strength and low density, but their utilization for high temperature service has been handicapped by their susceptibility to corrosion by atmospheric gases under some service conditions. At elevated temperatures both oxygen and nitrogen migrate from the surface into the interior of bodies of titanium and titanium base alloys, embrittling the whole structure. Moreover, titanium cannot be soldered, and is ditficult to draw, due to its tendency to gall or adhere strongly to drawing tools and dies.
  • the present invention comprises the discovery that coatings of aluminum, tin, copper, lead and other metals can be applied to a titanium base in such a way as to combine or alloy with the surface metal, thereby forming a permanently bonded protective and non-galling coating.
  • a copper coating can be secured by dipping for from to 35 seconds in fused cuprous chloride or an ad mixture thereof with other chlorides at a temperature of 650 C. to 700 C. Such coatings can be soldered.
  • a lead coating which enables wire and deep drawing can be secured by immersing for a few minutes in a lead bath at 870 C. to 925 C., the bath being cooled to 350 C. to 650 C.,, before the coated titanium is removed.
  • An adherent tin coating can be secured by immersing carefully cleaned titanium in molten tin at 780-790 C. for one or two minutes.
  • the preferred coating metal is aluminum.
  • the titanium body to be coated is first thoroughly cleaned, as by grit blasting, grinding or the like, degreased with carbon tetrachloride or the like, and is then immersed in a bath of molten aluminum, preferably at a temperature between about 725 C. and 900 C. At somewhat higher temperatures, say 1000 C., the molten aluminum attacks the titanium and forms a pasty sludge.
  • a protective salt, such as potassium chloride may be floated on the bath to minimize oxidation thereof.
  • a simplified flow diagram of the process is as follows, steps shown by dotted lines being alternatives in the step sequences shown by solid lines as indicated here- Patented July 11, 1961 ICC
  • the time of immersion varies with the bath temperatu-re. At 900 C., good coatings have been secured with times as short as 15 seconds and as long as seconds, While at 725 C., the time range is from 1 to 8 minutes. A time of about 4 minutes is preferred.
  • the coating secured by an immersion of 8 minutes is unnecessarily heavy, and some aluminum is lost by complete oxidation on subsequent exposure to high temperatures.
  • the uncoated control samples were completely converted to titanium-dioxide, showing a weight gain of about 81 mg./ sq. cm.
  • the specimen which had been immersed for 1 minute showed a weight gain of about 18 mg./sq. cm., and for 1 minute showed a weight gain of about 18 mg./sq. cm., and was coated With a removable tan scale.
  • the specimen which had been immersed for 2 minutes showed a weight gain somewhat over 20 mg./sq. cm., and was coated with a very adherent tan scale.
  • the specimens immersed for 4 and 8 minutes showed Weight gains of only about 9 mg./sq. sm., and were coated with very adherent gray scales.
  • the surfaces of all specimens were substantially hardened but toward the center hardness decreased rapidly.
  • Aluminum coatings can also be applied with beneficial results to titanium alloys which are embrittled by gas absorption at elevated temperatures.
  • an alloy of 10% maganese, 5% molybdenum, 5% chromium, balance titanium, as rolled and vacuum annealed showed a bend ductility of zero.
  • the aluminum-coated alloy still had a bend ductility of zero-T, while the bend ductility of the uncoated sample was 4 T.
  • the bend ductility of the uncoated specimen was 11 T, while that of the coated specimen remained at zero T.
  • the invention thus enables the use of titanium and its alloys at service temperature substantially higher than has heretofore been deemed possible.
  • the method of bonding a coating of aluminum onto atitanium base comprising the steps of thoroughly cleaning the surface of the titanium, and immersing the cleaned titanium in a bath of molten aluminum at a tem perature between 725 C. and 900 C. for a time between 15 seconds and 8 minutes.
  • the method of bonding a coating of aluminum onto a titanium base comprising the steps of thoroughly cleaning the surface of the titanium, and immersing the cleaned titanium in a bath of molten aluminum at a temperature of about 725 C. for a time between 1 minute and 8 minutes.
  • the method of bonding a coating of aluminum onto a titanium base comprising the steps of thoroughly cleaning the surface of the titanium, and immersing the cleaned titanium in a bath of molten aluminum at a temperature of about 900 C. for a time between 15 seconds and 90 seconds.
  • a method of drawing wire made of titanium and titanium-base alloys which comprises immersing said wire in a lead bath maintained at about 870 to 925 C. for an interval sufficient to form an adherent lead coat ing on said wire, cooling the so coated Wire below about 650 C., and drawing the same through a die of smaller sectional dimensions than the so coated Wire.
  • a method of drawing wire made of titanium and titanium-base alloys which comprises immersing said wire in a lead bath maintained at about 870 to 925 C. for an interval sufiicient to form an adherent lead coating on said wire, cooling the so coated wire to about 350 to 650 C., and drawing the same through a die of smaller sectional dimensions than the so coated wire.
  • the method of bonding a layer of metal selected from the group consisting of aluminum, tin, copper and lead onto a titanium base comprising the step of immersing the titanium base in a molten bath of said metals aluminum, tin and lead, respectively, and a fused bath of cuprous chloride for applying said coatings, respectively, and at a temperature at least 65 C. in excess of the melting point of said metal and between 650 C. and 925 C. for a time between 5 seconds and 8 minutes.
  • the method of bonding a coating of copper onto a titanium base comprising the step of immersing the titanium base in a molten bath containing cuprous chloride at a temperature between 650 C. and 700 C. for a time between 5 seconds and seconds.
  • the method of bonding a coating of lead onto a titanium base comprising the steps of immersing the titanium base in a molten bath of lead at a temperature between 870 C. and 925 C. for a predetermined time, subsequently cooling the bath to a temperature between 350 C. and 650 C. and then removing the coated titanium from the bath.
  • the method of bonding a coating of tin onto a titanium base comprising the step of immersing the titanium base in a molten bath of tin at a temperature between 780 C. and 790 C. for a time between 1 minute and 2 minutes.

Description

United States Patent O 2,992,135 REACTED COATING F TITANIUM Walter L. Finlay, Beaver, Pa., assignor, by mesne assignments, to Crucible Steel Company of America, Flemington, N.J., a corporation of New Jersey No Drawing. Original application '=0ct. 18, 1951, Ser. No. 251,979. Divided and this application Nov. 7, 1957, Ser. No. 694,934
9 Claims. (Cl. 117-114) The present invention is a division of my appplication Serial No. 251,979, filed October 18, 1951.
This invention relates to titanium and titanium base alloys, and contemplates materially enhancing the utility of these materials, particularly for high temperature service, by the use of coatings of other metals which bond themselves to the base metal by penetrating and alloying or combining therewith.
As structural materials, titanium and its alloys oifer a unique combination of high tensile strength and low density, but their utilization for high temperature service has been handicapped by their susceptibility to corrosion by atmospheric gases under some service conditions. At elevated temperatures both oxygen and nitrogen migrate from the surface into the interior of bodies of titanium and titanium base alloys, embrittling the whole structure. Moreover, titanium cannot be soldered, and is ditficult to draw, due to its tendency to gall or adhere strongly to drawing tools and dies.
The present invention comprises the discovery that coatings of aluminum, tin, copper, lead and other metals can be applied to a titanium base in such a way as to combine or alloy with the surface metal, thereby forming a permanently bonded protective and non-galling coating. A copper coating can be secured by dipping for from to 35 seconds in fused cuprous chloride or an ad mixture thereof with other chlorides at a temperature of 650 C. to 700 C. Such coatings can be soldered. A lead coating which enables wire and deep drawing can be secured by immersing for a few minutes in a lead bath at 870 C. to 925 C., the bath being cooled to 350 C. to 650 C.,, before the coated titanium is removed. An adherent tin coating can be secured by immersing carefully cleaned titanium in molten tin at 780-790 C. for one or two minutes.
The preferred coating metal is aluminum. The titanium body to be coated is first thoroughly cleaned, as by grit blasting, grinding or the like, degreased with carbon tetrachloride or the like, and is then immersed in a bath of molten aluminum, preferably at a temperature between about 725 C. and 900 C. At somewhat higher temperatures, say 1000 C., the molten aluminum attacks the titanium and forms a pasty sludge. A protective salt, such as potassium chloride, may be floated on the bath to minimize oxidation thereof.
A simplified flow diagram of the process is as follows, steps shown by dotted lines being alternatives in the step sequences shown by solid lines as indicated here- Patented July 11, 1961 ICC The time of immersion varies with the bath temperatu-re. At 900 C., good coatings have been secured with times as short as 15 seconds and as long as seconds, While at 725 C., the time range is from 1 to 8 minutes. A time of about 4 minutes is preferred. The coating secured by an immersion of 8 minutes is unnecessarily heavy, and some aluminum is lost by complete oxidation on subsequent exposure to high temperatures.
Specific examples of the practice of the invention are as follows:
Commercial titanium was rolled at a temperature of about 850 C. to a thickness of .030". Specimens cut from this sheet were cleaned by sand blasting and mechanical grinding, finally polishing on 600-grit paper, and degreasing in carbon tetrachloride. The specimens thus prepared were dipped in molten aluminum at a temperature of about 725 C., for times of 1,, 2, 4 and 8 minutes. All specimens received an adherent coating of aluminum, the coating being about .002 thick except on the 8 minute dip specimens, on which it was thicker. The coated specimens along with control samples of uncoated sheet were then heated in air for 24 hours at 1050 C. The uncoated control samples were completely converted to titanium-dioxide, showing a weight gain of about 81 mg./ sq. cm. The specimen which had been immersed for 1 minute showed a weight gain of about 18 mg./sq. cm., and for 1 minute showed a weight gain of about 18 mg./sq. cm., and was coated With a removable tan scale. The specimen which had been immersed for 2 minutes showed a weight gain somewhat over 20 mg./sq. cm., and was coated with a very adherent tan scale. The specimens immersed for 4 and 8 minutes showed Weight gains of only about 9 mg./sq. sm., and were coated with very adherent gray scales. The surfaces of all specimens were substantially hardened but toward the center hardness decreased rapidly.
Other specimens, prepared and coated as above, were heated in air for 24 hours at 850 C., with even more satisfactory results. The uncoated control samples showed a weight gain of about 9 mg./sq. cm., while the aluminized specimens gained from .09 to 2.5 mg./ sq. cm. The thickness of the aluminum oxide coating increased from about 2 mils to about 5 mils with increase in the immersion time. The oxide coating is relatively hard and is bonded to the titanium by a layer of about .5 mil thickness of an intermetallic compound having a hardness of about 250 Vickers-probably titanium-aluminum. This intermetallic layer shows plainly on micro-photographs of magnification. The original hardness (210 Vickers) of the titanium within the intermetallic bonding layer remains substantially unchanged. Ductility is not materially altered, and aluminum clad titanium can be cold rolled to 50% reduction without spalling or flaking.
Aluminum coatings can also be applied with beneficial results to titanium alloys which are embrittled by gas absorption at elevated temperatures. For example, an alloy of 10% maganese, 5% molybdenum, 5% chromium, balance titanium, as rolled and vacuum annealed, showed a bend ductility of zero. After air exposure at 300 C. for 60 hours, the aluminum-coated alloy still had a bend ductility of zero-T, while the bend ductility of the uncoated sample was 4 T. After air exposure at 900 C. for 5 minutes, the bend ductility of the uncoated specimen was 11 T, while that of the coated specimen remained at zero T.
The invention thus enables the use of titanium and its alloys at service temperature substantially higher than has heretofore been deemed possible.
What is claimed is:
1. The method of bonding a coating of aluminum onto atitanium base comprising the steps of thoroughly cleaning the surface of the titanium, and immersing the cleaned titanium in a bath of molten aluminum at a tem perature between 725 C. and 900 C. for a time between 15 seconds and 8 minutes.
2. The method of bonding a coating of aluminum onto a titanium base comprising the steps of thoroughly cleaning the surface of the titanium, and immersing the cleaned titanium in a bath of molten aluminum at a temperature of about 725 C. for a time between 1 minute and 8 minutes.
3. The method of bonding a coating of aluminum onto a titanium base comprising the steps of thoroughly cleaning the surface of the titanium, and immersing the cleaned titanium in a bath of molten aluminum at a temperature of about 900 C. for a time between 15 seconds and 90 seconds.
4. A method of drawing wire made of titanium and titanium-base alloys which comprises immersing said wire in a lead bath maintained at about 870 to 925 C. for an interval sufficient to form an adherent lead coat ing on said wire, cooling the so coated Wire below about 650 C., and drawing the same through a die of smaller sectional dimensions than the so coated Wire.
5. A method of drawing wire made of titanium and titanium-base alloys which comprises immersing said wire in a lead bath maintained at about 870 to 925 C. for an interval sufiicient to form an adherent lead coating on said wire, cooling the so coated wire to about 350 to 650 C., and drawing the same through a die of smaller sectional dimensions than the so coated wire.
6. The method of bonding a layer of metal selected from the group consisting of aluminum, tin, copper and lead onto a titanium base comprising the step of immersing the titanium base in a molten bath of said metals aluminum, tin and lead, respectively, and a fused bath of cuprous chloride for applying said coatings, respectively, and at a temperature at least 65 C. in excess of the melting point of said metal and between 650 C. and 925 C. for a time between 5 seconds and 8 minutes.
7. The method of bonding a coating of copper onto a titanium base comprising the step of immersing the titanium base in a molten bath containing cuprous chloride at a temperature between 650 C. and 700 C. for a time between 5 seconds and seconds.
8. The method of bonding a coating of lead onto a titanium base comprising the steps of immersing the titanium base in a molten bath of lead at a temperature between 870 C. and 925 C. for a predetermined time, subsequently cooling the bath to a temperature between 350 C. and 650 C. and then removing the coated titanium from the bath.
9. The method of bonding a coating of tin onto a titanium base comprising the step of immersing the titanium base in a molten bath of tin at a temperature between 780 C. and 790 C. for a time between 1 minute and 2 minutes.
References Cited in the file of this patent UNITED STATES PATENTS 141,132 Gauduin et al. July 22, 1873 2,082,622 Fink June 1, 1937 2,374,926 Fink May 1, 1945 2,398,738 Gilbert Apr. 16, 1946 2,586,142 Bailey et a1 Feb. 19, 1952 2,706,161 Westby Apr. 12, 1955 2,903,785 Hauink et a1 Sept. 15, 1959 2,930,106 Wrotnowski Nov. 29, 1960

Claims (1)

  1. 6. THE METHOD OF BONDING A LAYER OF METAL SELECTED FROM THE GROUP CONSISTING OF ALUMINUM, TIN, COPPER AND LEAD ONTO A TITANIUM BASE COMPRISING THE STEP OF IMMERSING THE TITANIUM BASE IN A MOLTEN BASE OF SAID METALS ALUMINUM, TIN AND LEAD, RESPECTIVELY, AND A FUSED BATH OF CUPROUS CHLORIDE FOR APPLYING SAID COATINGS, RESPECTIVELY, AND AT A TEMPERATURE AT LEAST 65*C. IN EXCESS OF THE MELTING POINT OF SAID METAL AND BETWEEN 650*C. AND 925*C. FOR A TIME BETWEEN 5 SECONDS AND 8 MINUTES.
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US251979A US3045333A (en) 1951-10-18 1951-10-18 Titanium coated article
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3156978A (en) * 1953-02-16 1964-11-17 Gen Motors Corp Joining titanium and titanium-base alloys to high melting metals
US3186070A (en) * 1961-07-03 1965-06-01 Gen Electric Protective coatings and process for producing the same
US3213532A (en) * 1961-04-03 1965-10-26 Westinghouse Electric Corp Method of forming titanium and aluminum seals
US3339271A (en) * 1964-07-01 1967-09-05 Wyman Gordon Co Method of hot working titanium and titanium base alloys
US3409978A (en) * 1965-08-17 1968-11-12 Gen Electric Metal cladding process
US3429158A (en) * 1966-11-28 1969-02-25 Atomic Energy Commission Protective cladding and lubricant for mechanically deformable reactive metals
US3640778A (en) * 1969-03-27 1972-02-08 United Aircraft Corp Coating of titanium alloys
US3890818A (en) * 1972-03-16 1975-06-24 Cefilac Process for hot extruding metals
US4197360A (en) * 1978-05-01 1980-04-08 The United States Of America As Represented By The Secretary Of The Army Multilayer laminate of improved resistance to fatigue cracking
US5580669A (en) * 1994-02-17 1996-12-03 United Technologies Corporation Oxidation resistant coating for titanium alloys
US5672436A (en) * 1990-05-31 1997-09-30 Grumman Aerospace Corporation Oxidation protection method for titanium
US5765418A (en) * 1994-05-16 1998-06-16 Medtronic, Inc. Method for making an implantable medical device from a refractory metal

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US141132A (en) * 1873-07-22 Improvement in coating metals with copper
US2082622A (en) * 1933-02-25 1937-06-01 Colin G Fink Daluminum coated metal and process for producing the same
US2374926A (en) * 1941-10-11 1945-05-01 Colin G Fink Process of coating with tin or other metals
US2398738A (en) * 1943-12-28 1946-04-16 Du Pont Process of metal coating light metals
US2586142A (en) * 1947-11-10 1952-02-19 British Non Ferrous Metals Res Process for the production of lead coatings
US2706161A (en) * 1950-12-29 1955-04-12 Thor H Westby Flux for aluminum coating of ferrous materials and process of coating therewith
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US5776266A (en) * 1990-05-31 1998-07-07 Northrop Grumman Corporation Oxidation protection method for titanium
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