US3045333A - Titanium coated article - Google Patents

Titanium coated article Download PDF

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Publication number
US3045333A
US3045333A US251979A US25197951A US3045333A US 3045333 A US3045333 A US 3045333A US 251979 A US251979 A US 251979A US 25197951 A US25197951 A US 25197951A US 3045333 A US3045333 A US 3045333A
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Prior art keywords
titanium
aluminum
coated
base
article
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US251979A
Inventor
Walter L Finlay
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Rem Cru Titanium Inc
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Rem Cru Titanium Inc
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Priority to US251979A priority Critical patent/US3045333A/en
Priority to US694934A priority patent/US2992135A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/12Aluminium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/923Physical dimension
    • Y10S428/924Composite
    • Y10S428/926Thickness of individual layer specified
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/939Molten or fused coating
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12687Pb- and Sn-base components: alternative to or next to each other
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12736Al-base component
    • Y10T428/12743Next to refractory [Group IVB, VB, or VIB] metal-base component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12806Refractory [Group IVB, VB, or VIB] metal-base component

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 ofier As structural materials, titanium and its alloys ofier 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 diiiicult 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 app-lied 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 5 to 35 seconds in fused cuprous chloride or an admixture 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's'ecured 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.,
  • An adherent tin coating can be secured by immersing carefully cleaned titanium in molten tin at 780-790 C. for one or tw minutes.
  • the preferred coating metal is aluminum.
  • the titanium body to be coated is first thoroughly cleaned, as by grit blastinggrinding or the like, degreased with carbon tetcachloride 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 1'000 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.
  • the time of immersion varies with the bath temperature. At 900 C., good coatings have been secured with times as short as seconds and as long as 90 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 rug/sq. cm.
  • the specimen which had been immersed 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 rug/sq. cm., 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% manganese, 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 unv coated sample was 4T. After air exposure at 900 C.
  • the specimens The invention thus enables the use of titanium and its alloys at service temperatures substantially higher than has heretofore been deemed possible.
  • a layer of a metal selected from the group consisting of aluminum, tin, copper and lead said layer being bonded to the titanium by an intermetallic compound of titanium and the selected metal.
  • a metal article protected from surface deterioration at elevated operating temperatures comprising a base consisting predominantly of titanium and a protective layer on said base of a metal selected from the group consisting of aluminum, tin, copper and lead, said layer being substantially continuous and bonded to said base.
  • a metallic article protected from surface deterioration at elevated operating temperatures comprising a base consisting predominantly of titanium and a protective layer on said base of aluminum, said layer being substantially continuous and bonded to said base.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Coating With Molten Metal (AREA)

Description

3,045,333 TlTANlIUM CGATED ARTICLE Walter. L. Finlay, Beaver, Pa., assignor to Rem-Cm Titanium, Inc, Midland, lPa., a corporation of Pennsylvania No Drawing. Filed Oct. 18, 1951, Ser. No. 251,979
, 4- Claims. (Cl. 29-194) 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 ofier 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 diiiicult 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 app-lied 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 5 to 35 seconds in fused cuprous chloride or an admixture 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's'ecured 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 tw minutes.
The preferred coating metal is aluminum. The titanium body to be coated is first thoroughly cleaned, as by grit blastinggrinding or the like, degreased with carbon tetcachloride 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 1'000 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.
The time of immersion varies with the bath temperature. At 900 C., good coatings have been secured with times as short as seconds and as long as 90 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,
coated sheet were then heated in air for 24 hours at 105 0 C. The uncoated control samples were completely converted to titanium-dioxide, showing a weight gain of about 81 rug/sq. cm. The specimen which had been immersed 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 rug/sq. cm., 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 rug/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 100 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 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% manganese, 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 unv coated sample was 4T. After air exposure at 900 C.
for 5 minutes, the bend ductility of the uncoated specimen was 11T, while that of the coated specimen remained at zero-T.
and degreasing in carbon tetrachloride. The specimens The invention thus enables the use of titanium and its alloys at service temperatures substantially higher than has heretofore been deemed possible.
What is claimed is:
1. An article of titanium surface-coated with aluminum, the surface coating being bonded to the titanium base by an interfacial layer of the reaction product secured by immersing the clean titanium article in molten aluminum.
2. An article consisting predominantly of titanium,
surface coated with a layer of a metal selected from the group consisting of aluminum, tin, copper and lead, said layer being bonded to the titanium by an intermetallic compound of titanium and the selected metal.
3. A metal article protected from surface deterioration at elevated operating temperatures comprising a base consisting predominantly of titanium and a protective layer on said base of a metal selected from the group consisting of aluminum, tin, copper and lead, said layer being substantially continuous and bonded to said base.
4. A metallic article protected from surface deterioration at elevated operating temperatures comprising a base consisting predominantly of titanium and a protective layer on said base of aluminum, said layer being substantially continuous and bonded to said base.
(References on following page) Fatentecl July 24., 19oz References Cited in the file of this patent UNITED STATES PATENTS Thowless Jan. 5, 1915 Kirby Jan. 26, 1915 Austin Jan. 16, 1934 Pink June 1, 1937 Charlton June 1, 1937 Scheller Mar. 21, 1939 Whitfield et a1. Aug. 1, 1939 Scott Oct. 10, 1939 Ball June 17, 1941 Taylor May 5, 1942 4 Pink May 1, 1945 Whitfield et a1. Dec. 7, 1948 Thomas et a1. Mar. 22, 1949 Spence Aug. 23, 1949 Sears Dec. 13, 1949 Fink Feb. 14, 1950 Jenks Oct. 10, 1950 Apker June 12, 1951 Brennan Sept. 25, 1951 Alexander Apr. 6, 1954 Whitfield June 29, 1954 Pink July 6, 1954 Wainer Sept. 28, 1954

Claims (1)

1. AN ARTICLE OF TITANIUM SURFACE-COATED WITH ALUMINUM, THE SURFACE COATING BEING BONDED TO THE TITANIUM BASE BY AN INTERFACIAL LAYER OF THE REACTION PRODUCT SECURED BY IMMERSING THE CLEAN TITANIUM ARTICLE IN MOLTEN ALUMINUM.
US251979A 1951-10-18 1951-10-18 Titanium coated article Expired - Lifetime US3045333A (en)

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US694934A US2992135A (en) 1951-10-18 1957-11-07 Reacted coating of titanium

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3233312A (en) * 1962-08-03 1966-02-08 Du Pont Explosively bonded product
US3297552A (en) * 1963-02-25 1967-01-10 Gisser Henry Method of making a titanium piece having good anti-wear, anti-galling, antiseizure and anti-friction properties
US3434813A (en) * 1964-12-07 1969-03-25 Crucible Steel Co America Composite titanium-alloy article resistant to hot salt corrosion
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
US4681818A (en) * 1986-03-18 1987-07-21 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Oxygen diffusion barrier coating
US5300159A (en) * 1987-12-23 1994-04-05 Mcdonnell Douglas Corporation Method for manufacturing superplastic forming/diffusion bonding tools from titanium
US5580669A (en) * 1994-02-17 1996-12-03 United Technologies Corporation Oxidation resistant coating for titanium alloys

Citations (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1123625A (en) * 1915-01-05 O M Thowless Glower for electrical incandescent lamps.
US1126484A (en) * 1913-11-28 1915-01-26 John Kirby Method of manufacturing composite metallic articles.
US1943853A (en) * 1930-10-31 1934-01-16 Fansteel Prod Co Inc Biplate metal
US2082622A (en) * 1933-02-25 1937-06-01 Colin G Fink Daluminum coated metal and process for producing the same
US2082685A (en) * 1935-07-16 1937-06-01 Henry Disston & Sons Inc File and like tool
US2151302A (en) * 1936-06-26 1939-03-21 Reynolds Metals Co Tin alloy
US2167701A (en) * 1936-09-21 1939-08-01 Reynolds Metals Co Method of producing aluminum treated articles of iron
US2175706A (en) * 1938-10-25 1939-10-10 Continental Steel Corp Galvanizing sheets of metal
US2245745A (en) * 1939-07-12 1941-06-17 Ball Chemical Company Metallic coating
US2282097A (en) * 1940-03-29 1942-05-05 Warren G Taylor Nonemitting electrode structure
US2374926A (en) * 1941-10-11 1945-05-01 Colin G Fink Process of coating with tin or other metals
US2455457A (en) * 1941-10-24 1948-12-07 Fairchild Engine & Airplane Coated metal article
US2464836A (en) * 1944-08-24 1949-03-22 Arcos Corp Welding
US2479979A (en) * 1945-07-25 1949-08-23 Hooker Electrochemical Co Processes for treating ferrous metals before drawing through dies
US2491284A (en) * 1946-12-13 1949-12-13 Bell Telephone Labor Inc Electrode for electron discharge devices and method of making the same
US2497119A (en) * 1944-09-18 1950-02-14 Alwac Company Inc Method of coating ferrous metals with aluminum
US2525603A (en) * 1945-11-21 1950-10-10 Revere Copper & Brass Inc Method of making lead coated copper
US2556864A (en) * 1950-09-27 1951-06-12 Gen Electric Coated grid for electron discharge tubes
US2569149A (en) * 1945-10-19 1951-09-25 Joseph B Brennan Bimetallic structure
US2674542A (en) * 1951-02-06 1954-04-06 Metal Hydrides Inc Method for producing hard surfaced titanium
US2682101A (en) * 1946-06-01 1954-06-29 Whitfield & Sheshunoff Inc Oxidation protected tungsten and molybdenum bodies and method of producing same
US2682702A (en) * 1949-04-06 1954-07-06 Ohio Commw Eng Co Carbonyl metal plated product
US2690409A (en) * 1949-07-08 1954-09-28 Thompson Prod Inc Binary coating of refractory metals

Patent Citations (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1123625A (en) * 1915-01-05 O M Thowless Glower for electrical incandescent lamps.
US1126484A (en) * 1913-11-28 1915-01-26 John Kirby Method of manufacturing composite metallic articles.
US1943853A (en) * 1930-10-31 1934-01-16 Fansteel Prod Co Inc Biplate metal
US2082622A (en) * 1933-02-25 1937-06-01 Colin G Fink Daluminum coated metal and process for producing the same
US2082685A (en) * 1935-07-16 1937-06-01 Henry Disston & Sons Inc File and like tool
US2151302A (en) * 1936-06-26 1939-03-21 Reynolds Metals Co Tin alloy
US2167701A (en) * 1936-09-21 1939-08-01 Reynolds Metals Co Method of producing aluminum treated articles of iron
US2175706A (en) * 1938-10-25 1939-10-10 Continental Steel Corp Galvanizing sheets of metal
US2245745A (en) * 1939-07-12 1941-06-17 Ball Chemical Company Metallic coating
US2282097A (en) * 1940-03-29 1942-05-05 Warren G Taylor Nonemitting electrode structure
US2374926A (en) * 1941-10-11 1945-05-01 Colin G Fink Process of coating with tin or other metals
US2455457A (en) * 1941-10-24 1948-12-07 Fairchild Engine & Airplane Coated metal article
US2464836A (en) * 1944-08-24 1949-03-22 Arcos Corp Welding
US2497119A (en) * 1944-09-18 1950-02-14 Alwac Company Inc Method of coating ferrous metals with aluminum
US2479979A (en) * 1945-07-25 1949-08-23 Hooker Electrochemical Co Processes for treating ferrous metals before drawing through dies
US2569149A (en) * 1945-10-19 1951-09-25 Joseph B Brennan Bimetallic structure
US2525603A (en) * 1945-11-21 1950-10-10 Revere Copper & Brass Inc Method of making lead coated copper
US2682101A (en) * 1946-06-01 1954-06-29 Whitfield & Sheshunoff Inc Oxidation protected tungsten and molybdenum bodies and method of producing same
US2491284A (en) * 1946-12-13 1949-12-13 Bell Telephone Labor Inc Electrode for electron discharge devices and method of making the same
US2682702A (en) * 1949-04-06 1954-07-06 Ohio Commw Eng Co Carbonyl metal plated product
US2690409A (en) * 1949-07-08 1954-09-28 Thompson Prod Inc Binary coating of refractory metals
US2556864A (en) * 1950-09-27 1951-06-12 Gen Electric Coated grid for electron discharge tubes
US2674542A (en) * 1951-02-06 1954-04-06 Metal Hydrides Inc Method for producing hard surfaced titanium

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3233312A (en) * 1962-08-03 1966-02-08 Du Pont Explosively bonded product
US3297552A (en) * 1963-02-25 1967-01-10 Gisser Henry Method of making a titanium piece having good anti-wear, anti-galling, antiseizure and anti-friction properties
US3434813A (en) * 1964-12-07 1969-03-25 Crucible Steel Co America Composite titanium-alloy article resistant to hot salt corrosion
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
US4681818A (en) * 1986-03-18 1987-07-21 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Oxygen diffusion barrier coating
US5300159A (en) * 1987-12-23 1994-04-05 Mcdonnell Douglas Corporation Method for manufacturing superplastic forming/diffusion bonding tools from titanium
US5580669A (en) * 1994-02-17 1996-12-03 United Technologies Corporation Oxidation resistant coating for titanium alloys

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