EP1784269B1 - Method for manufacturing titanium alloy wire with enhanced properties - Google Patents

Method for manufacturing titanium alloy wire with enhanced properties Download PDF

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Publication number
EP1784269B1
EP1784269B1 EP05755493A EP05755493A EP1784269B1 EP 1784269 B1 EP1784269 B1 EP 1784269B1 EP 05755493 A EP05755493 A EP 05755493A EP 05755493 A EP05755493 A EP 05755493A EP 1784269 B1 EP1784269 B1 EP 1784269B1
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EP
European Patent Office
Prior art keywords
titanium alloy
wire
reduction
tib
billet
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 - Fee Related
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EP05755493A
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German (de)
French (fr)
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EP1784269A4 (en
EP1784269A2 (en
Inventor
William M. Hanusiak
Jerry L. Fields
Vincent Harold Hammond
Robert Lewis Grabow
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FMW Composite Systems Inc
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FMW Composite Systems Inc
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Publication of EP1784269A2 publication Critical patent/EP1784269A2/en
Publication of EP1784269A4 publication Critical patent/EP1784269A4/en
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/17Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces by forging
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • C22C1/1042Alloys containing non-metals starting from a melt by atomising
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21CMANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES OR PROFILES, OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
    • B21C1/00Manufacture of metal sheets, metal wire, metal rods, metal tubes by drawing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/10Sintering only
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F5/00Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product
    • B22F5/12Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product of wires
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • B22F2998/10Processes characterised by the sequence of their steps

Definitions

  • the present invention relates to a method of manufacturing titanium alloy wire and, more particularly, to such a method wherein precipitated discontinuous particulates of a TiB reinforcement material, possibly also TiC, are added to the alloy and it is processed in accordance with a new and improved method wherein the reinforcement thereof by the particulates is enhanced.
  • the new and improved method of the present invention is not subject to these disadvantages and possesses advantages not possible with the use of previously used or known methods.
  • the document US-A-5 141 566 discloses a method for producing a titanium alloy wire.
  • the method of the present invention is directed to the manufacturing of titanium alloy wire suitable for application to wire/fiber composites, generally comprising the steps of forming the desired alloy via casting a billet or gas atomization; hot forging to create a uniform chemistry and microstructure; conforming to rod or coil, e.g., of about 5.08 mm (0.2 inches) in diameter; and cold drawing to wire, e.g., of about 0.127 mm (.005 inches) in diameter.
  • a preferred method comprises the formation of titanium alloy powder by gas atomization from a boron rich melt; consolidating the powder metal to bar form using hot isostatic pressing (HIP) with a pressure of 34.5 MPa to 310.3 MPa (5,000 to 45,000 psi), e.g., 103.4 MPa (15,000 psi), and a temperature of 898.9°C to 954.4°C (1,650°F to 1,750°F) until full consolidation, yet remaining below the beta transis to avoid grain growth and grain boundary segregation; hot reduction at 815.5°C to 1148.9°C (1500°F to 2100°F), e.g., 954.4°C (1,750°F), to reduce the bar to rod or coil form and perform the initial break-up of the larger TiB grains; and cold drawing and annealing at approximately a 10 to 20 percent reduction per pass to avoid cracking.
  • HIP hot isostatic pressing
  • an increased frequency of annealing steps under very low oxygen conditions serves to relieve work hardening and also recrystallizes the TiB grains to a refined size with alignment with the wire axis.
  • This new and improved method enables the fabrication of fine titanium alloy wire with simultaneous achievement of high TiB reinforcement content and small reinforcement grain size.
  • Other reinforcement materials may be used such as TiC, alone or in combination with TiB.
  • the method of the present invention has been developed to achieve predominately fine grained reinforcement even at high reinforcement content through the combination of precipitation of reinforcement and a new and improved wire fabrication method.
  • Typical fine wire processing practice suitable for application to wire/fiber composites such as described in U.S. Patent No. 5,763,079 , consists of four principal operations, namely, formation of the desired alloy via casting a billet, hot forging to create a uniform chemistry and microstructure, hot forming to rod (or coil) of about 5.08 mm (0.2 inches) in diameter, and cold drawing to wire of about .005 inches in diameter. Intermediate annealing operations are necessary during the cold drawing to relieve residual stresses and restore ductility for further drawing.
  • This basic wire forming process is designed to achieve area reduction through hot forming, hot extrusion and finally cold drawing in the fewest operations and the fewest breaks that would affect continuous lengths.
  • the wire drawing process can be designed or modified to control microstructural evolution in addition to the base purpose of area reduction.
  • the wire drawing method of the present invention can achieve improved microstructures in difficult alloys that cannot be achieved by any other known method, and was developed for the purpose of producing a discontinuously reinforced Ti-6Al-4V alloy with the simultaneous achievement of high TiB content and small reinforcement grain size.
  • the present wire forming method can start with a casting of Ti-6A1-4V alloy from a Boron rich melt.
  • the TiB will precipitate during cooling, but the cooling rate will allow for larger TiB grain growth which is undesirable.
  • a powder metal formed by gas atomization from a Boron rich melt preferably is used rather than a casting.
  • the powder forming process employs more rapid cooling than casting and is less likely to produce large TiB grains.
  • a compositionally uniform billet is prepared using powder metallurgy techniques to avoid the grain growth and potential for chemical segregation inherent in the casting process.
  • the metal alloy powder produced from Boron rich Ti-6A1-4V alloy is first hot formed into a bar compatible in size with the available industrial wire forming equipment. The bar is hot rolled into rod or coil with a diameter of about 5.08 mm (0.2 inches), and the rod or coil is then transferred to the cold drawing operations.
  • the cold drawing process of the present invention serves to break up the large TiB grains without deleterious microcracking or void formation. It has been discovered that the addition of frequent annealing steps to relieve work hardening will also recrystallize the TiB grains to a refined size with alignment with the wire axis. Annealing steps have been utilized in the known wire drawing process, but less frequently and for shorter periods of time. The increased frequency of anneals in accordance with the present invention increases the requirement for annealing under very low oxygen conditions to avoid excessive surface material loss due to oxygen contamination and oxygen interstitial pick up by the wire metallurgy that may interfere with the TiB refinement process. Accordingly, the present method enables the fabrication of fine titanium alloy wire with simultaneous achievement of high reinforcement content and small reinforcement grain size.
  • an acceptable alloy powder is gas atomized spherical powder with a composition of Ti-6A1-4V-1.7B in a size range of minus 35 mesh to plus 270 mesh.
  • An acceptable interstitial content was found to be oxygen less than 1500 ppm.
  • This quality powder has been used to fabricate composite panels and is known to yield uniform chemistry and microstructure. Consolidation of the powder metal to bar form is based on methods found successful for composite panels. For example, it has been determined that non-contaminating consolidation tooling is needed, such as vacuum degassed mild steel or conventional titanium alloys.
  • Consolidation to a bar is achieved using hot isostatic pressing (HIP) with a pressure of 34.5 MPa to 310.3 MPa (5000 psi to 45,000 psi), e.g., 103.4 MPa (15,000 psi), and a temperature of 898.9°C to 954.4°C (1650°F to 1750°F).
  • HIP hot isostatic pressing
  • the hot reduction operation at 815.5°C to 1148.9°C (1500°F to 2100°F), e.g., 954.4°C (1750°F) serves to reduce the bar to coil or rod form and performs the initial breakup to the larger TiB grains.
  • Annealing at about 648.9°C to 1093.3°C (1200°F to 2000°F), e.g., 954.4°C (1750°F) for 1 hour in inert gas with forced inert gas cooling is sufficient to remove work hardening, recrystallize the TiB and avoid grain growth.
  • Annealing is performed at intervals corresponding to an accumulated reduction in section area of 50 percent.
  • the above-described method of the present invention produces Ti-6A1-4V alloy with fine grained TiB reinforcement in concentrations ranging from 1 to 50 percent by volume with reinforcement alignment along the wire axis. It has been found that this process is effective with a wide variety of titanium alloys, such as Ti-6A1-2Sn-4Zr-2Mo alloy, Ti-6Al-4Sn-4Zr-1Nb-1Mo-0.2Si alloy, Ti-3Al-2.5V alloy, Ti-10V-2Fe-3Al alloy, Ti-5Al-2.5 Sn alloy and Ti-8Al-1Mo-1V alloy. Also, it is effective with other precipitated discontinuous reinforcements such as TiC.
  • the method may utilize a billet cast from a Boron rich melt, but the inherent risks of microcracking and void formation would be greater owing to the larger TiB grain growth that results from a slow cooled casting.
  • the extremely high area reductions inherent in the wire forming process combined with properly controlled reduction and annealing conditions in the present method produces high performance titanium alloy wire that cannot be produced by any other known metallurgical process.

Abstract

A method for producing reinforced titanium alloy wire, comprising forming a billet of titanium alloy with grains of a precipitated discontinuous reinforcement material such as TiB and/or TiC. The billet may be formed by the hot consolidation of a titanium alloy powder formed by gas atomization. The billet is then hot formed to reduce it to rod or coil form. The rod or coil is then subjected to successive cold drawing operations to form a reinforced titanium alloy wire of reduced diameter. The cold drawing includes periodic annealing operations under low oxygen conditions to relieve work hardening and to recrystallize the reinforcement material grains to reduce the size thereof.

Description

    Field of the Invention
  • The present invention relates to a method of manufacturing titanium alloy wire and, more particularly, to such a method wherein precipitated discontinuous particulates of a TiB reinforcement material, possibly also TiC, are added to the alloy and it is processed in accordance with a new and improved method wherein the reinforcement thereof by the particulates is enhanced.
  • Background of the Invention
  • [Processes have been reported in the literature in which a common alloy of titanium, Ti-6A1-4V, has been reinforced and enhanced by the addition of TiB and/or TiC particulates (see US-A-4 731 115 ). This is significant in that the Ti-6A1-4V alloy is utilized extensively in aerospace applications and is one of the most affordable. Enhancements that enable the extension of the useful application range of such alloys without significant cost impact are of great interest to the aerospace design community. In the reported processes, a Ti-6A1-4V casting was produced with TiB and/or TiC additions being added to the melt before casting. These additions dissolve in the melt and recrystallize during cooling to form discontinuous reinforcement in a variety of sizes. Articles compacted by hot isostatic pressing (HIP) and extrusion have demonstrated improved tensile strength and tensile modulus depending on the concentrations of TiB and/or TiC additions.
  • The results indicate that improvements in properties are related to the amount of discontinuous reinforcement created and to the size of the resulting reinforcement crystals. That is, it is desirable to have the reinforcement content as high as 40% by volume and the reinforcement size to be in the ultra fine size range. In the known processes, however, reinforcement content above a few percent is predominately in the largest size fraction with wide variability in size distribution and the shift to larger sized reinforcement is exaggerated as the reinforcement content increases toward the most desirable levels between 20 to 40% by volume. This is the result of large grains scavenging smaller grains during the casting or fabrication process and is apparently inherent in such processes. This limitation seriously inhibits the full capability of the discontinuously reinforced titanium potential.
  • The new and improved method of the present invention is not subject to these disadvantages and possesses advantages not possible with the use of previously used or known methods.
  • The document US-A-5 141 566 discloses a method for producing a titanium alloy wire.
  • Summary of the Invention
  • The method of the present invention, which is defined in claim 1, is directed to the manufacturing of titanium alloy wire suitable for application to wire/fiber composites, generally comprising the steps of forming the desired alloy via casting a billet or gas atomization; hot forging to create a uniform chemistry and microstructure; conforming to rod or coil, e.g., of about 5.08 mm (0.2 inches) in diameter; and cold drawing to wire, e.g., of about 0.127 mm (.005 inches) in diameter.
  • More specifically, a preferred method comprises the formation of titanium alloy powder by gas atomization from a boron rich melt; consolidating the powder metal to bar form using hot isostatic pressing (HIP) with a pressure of 34.5 MPa to 310.3 MPa (5,000 to 45,000 psi), e.g., 103.4 MPa (15,000 psi), and a temperature of 898.9°C to 954.4°C (1,650°F to 1,750°F) until full consolidation, yet remaining below the beta transis to avoid grain growth and grain boundary segregation; hot reduction at 815.5°C to 1148.9°C (1500°F to 2100°F), e.g., 954.4°C (1,750°F), to reduce the bar to rod or coil form and perform the initial break-up of the larger TiB grains; and cold drawing and annealing at approximately a 10 to 20 percent reduction per pass to avoid cracking. In accordance with the method of the present invention, an increased frequency of annealing steps under very low oxygen conditions serves to relieve work hardening and also recrystallizes the TiB grains to a refined size with alignment with the wire axis. This new and improved method enables the fabrication of fine titanium alloy wire with simultaneous achievement of high TiB reinforcement content and small reinforcement grain size. Other reinforcement materials may be used such as TiC, alone or in combination with TiB.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The method of the present invention has been developed to achieve predominately fine grained reinforcement even at high reinforcement content through the combination of precipitation of reinforcement and a new and improved wire fabrication method. Typical fine wire processing practice suitable for application to wire/fiber composites, such as described in U.S. Patent No. 5,763,079 , consists of four principal operations, namely, formation of the desired alloy via casting a billet, hot forging to create a uniform chemistry and microstructure, hot forming to rod (or coil) of about 5.08 mm (0.2 inches) in diameter, and cold drawing to wire of about .005 inches in diameter. Intermediate annealing operations are necessary during the cold drawing to relieve residual stresses and restore ductility for further drawing. This basic wire forming process is designed to achieve area reduction through hot forming, hot extrusion and finally cold drawing in the fewest operations and the fewest breaks that would affect continuous lengths.
  • In accordance with the present invention, it has been discovered that the wire drawing process can be designed or modified to control microstructural evolution in addition to the base purpose of area reduction. The wire drawing method of the present invention can achieve improved microstructures in difficult alloys that cannot be achieved by any other known method, and was developed for the purpose of producing a discontinuously reinforced Ti-6Al-4V alloy with the simultaneous achievement of high TiB content and small reinforcement grain size.
  • The present wire forming method can start with a casting of Ti-6A1-4V alloy from a Boron rich melt. The TiB will precipitate during cooling, but the cooling rate will allow for larger TiB grain growth which is undesirable. In order to start with the best microstructure, a powder metal formed by gas atomization from a Boron rich melt preferably is used rather than a casting. The powder forming process employs more rapid cooling than casting and is less likely to produce large TiB grains. In this method, a compositionally uniform billet is prepared using powder metallurgy techniques to avoid the grain growth and potential for chemical segregation inherent in the casting process. The metal alloy powder produced from Boron rich Ti-6A1-4V alloy is first hot formed into a bar compatible in size with the available industrial wire forming equipment. The bar is hot rolled into rod or coil with a diameter of about 5.08 mm (0.2 inches), and the rod or coil is then transferred to the cold drawing operations.
  • It has been discovered that selection of correct cold drawing processing conditions results in ductile small diameter fine wire and a successful evolution of the desired wire microstructure, that is, high concentrations and fine grains. Execution of this improved process requires consideration of critical processing conditions in each operation. Cold drawing area reduction must be sufficient to cold work the small diameter rods to the core on each pass in order to maintain micro-structural uniformity throughout the cross section. The reduction in area must not be excessive, however, to avoid fracture, microcracking or void formation within the rod or coil as it is reduced in diameter. The presence of the large TiB grains in the initial stages of cold drawing make the material susceptible to microcracking and void formation in the region of the large TiB grains. This balance between area reduction and avoidance of microcracking and void formation is more difficult in the beginning of the reduction sequence when the largest TiB grains are present, and the processing window expands as the TiB grain size is reduced.
  • The cold drawing process of the present invention serves to break up the large TiB grains without deleterious microcracking or void formation. It has been discovered that the addition of frequent annealing steps to relieve work hardening will also recrystallize the TiB grains to a refined size with alignment with the wire axis. Annealing steps have been utilized in the known wire drawing process, but less frequently and for shorter periods of time. The increased frequency of anneals in accordance with the present invention increases the requirement for annealing under very low oxygen conditions to avoid excessive surface material loss due to oxygen contamination and oxygen interstitial pick up by the wire metallurgy that may interfere with the TiB refinement process. Accordingly, the present method enables the fabrication of fine titanium alloy wire with simultaneous achievement of high reinforcement content and small reinforcement grain size.
  • In accordance with a preferred embodiment of the method of the present invention, an acceptable alloy powder is gas atomized spherical powder with a composition of Ti-6A1-4V-1.7B in a size range of minus 35 mesh to plus 270 mesh. An acceptable interstitial content was found to be oxygen less than 1500 ppm. This quality powder has been used to fabricate composite panels and is known to yield uniform chemistry and microstructure. Consolidation of the powder metal to bar form is based on methods found successful for composite panels. For example, it has been determined that non-contaminating consolidation tooling is needed, such as vacuum degassed mild steel or conventional titanium alloys. Consolidation to a bar is achieved using hot isostatic pressing (HIP) with a pressure of 34.5 MPa to 310.3 MPa (5000 psi to 45,000 psi), e.g., 103.4 MPa (15,000 psi), and a temperature of 898.9°C to 954.4°C (1650°F to 1750°F). These conditions serve to achieve full consolidation and yet remain safely below the beta transis to avoid grain growth and grain boundary segregation. The hot reduction operation at 815.5°C to 1148.9°C (1500°F to 2100°F), e.g., 954.4°C (1750°F), serves to reduce the bar to coil or rod form and performs the initial breakup to the larger TiB grains. It has been determined that about 50:1 hot reduction in section area is effective to breakup of the primary large TiB grains. The subsequent cold drawing must impart sufficient cold work through the thickness of the rod or coil, and the annealing must relieve the work hardening without grain growth. It has been determined that about a 10 percent reduction per pass is necessary to assure sufficient uniformity of cold worsting and avoid microcracking and void formation during the initial cold drawing steps from the nominal 5.08 mm (0.2 inch) diameter condition. Reductions in area can increase to about 15 percent per pass by the mid-point in the sectional area reduction process, and about 20 percent area reductions are possible by the end of the area reduction process. Annealing at about 648.9°C to 1093.3°C (1200°F to 2000°F), e.g., 954.4°C (1750°F) for 1 hour in inert gas with forced inert gas cooling is sufficient to remove work hardening, recrystallize the TiB and avoid grain growth. Annealing is performed at intervals corresponding to an accumulated reduction in section area of 50 percent.
  • The above-described method of the present invention produces Ti-6A1-4V alloy with fine grained TiB reinforcement in concentrations ranging from 1 to 50 percent by volume with reinforcement alignment along the wire axis. It has been found that this process is effective with a wide variety of titanium alloys, such as Ti-6A1-2Sn-4Zr-2Mo alloy, Ti-6Al-4Sn-4Zr-1Nb-1Mo-0.2Si alloy, Ti-3Al-2.5V alloy, Ti-10V-2Fe-3Al alloy, Ti-5Al-2.5 Sn alloy and Ti-8Al-1Mo-1V alloy. Also, it is effective with other precipitated discontinuous reinforcements such as TiC. The method may utilize a billet cast from a Boron rich melt, but the inherent risks of microcracking and void formation would be greater owing to the larger TiB grain growth that results from a slow cooled casting. The extremely high area reductions inherent in the wire forming process combined with properly controlled reduction and annealing conditions in the present method produces high performance titanium alloy wire that cannot be produced by any other known metallurgical process.

Claims (6)

  1. A method for producing reinforced titanium alloy wire, comprising:
    forming a powder of titanium alloy by gas atomization from a Boron rich melt;
    consolidating the titanium alloy powder under heat and pressure into a billet having grains of precipitated discontinuous TiB reinforcement, wherein said consolidating is by hot isostatic pressing at a pressure of 34.5 MPa to 310.3 MPa (5,000 to 45,000 psi) and a temperature of 898.9°C to 954.4°C (1650°F to 1750°F);
    hot forming the billet at a temperature of 815.5°C to 1148.9°C (1500°F to 2100°F), producing a 50:1 hot reduction in section area, to reduce the billet to rod or coil form and to break up and reduce the size of the TiB grains;
    cold drawing the rod or coil in successive operations to wire of reduced diameter;
    annealing the wire periodically at intervals corresponding to an accumulated reduction of section area of 50% for one hour in inert gas with forced inert gas cooling, to relieve work hardening and to recrystallize the TiB grains to reduce the size thereof.
  2. The method of claim 1, wherein said powder is gas atomized powder with a composition of Ti-6Al-4v-1.7B in a size range of minus 35 mesh to plus 270 mesh, with an interstitial content of oxygen less than 1500 ppm.
  3. The method of Claim 1, wherein said hot isostatic pressing is at a pressure of 103.4 MPa (15,000 psi).
  4. The method of claim 1 wherein said hot forming is at a temperature of 954.4°C (1750°F).
  5. The method of claim 1 wherein said cold drawing is performed periodically to reduce the size of the wire at a rate of approximately 10 percent for each drawing operation during the first half of accumulated reduction of the desired diameter reduction.
  6. The method of claim 5 wherein the rate of diameter reduction is increased to 15 percent for each drawing operation at the midpoint of accumulated reduction of the diameter reduction and to 20 percent prior to the end of the diameter reduction.
EP05755493A 2004-07-22 2005-05-25 Method for manufacturing titanium alloy wire with enhanced properties Expired - Fee Related EP1784269B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/895,885 US20060016521A1 (en) 2004-07-22 2004-07-22 Method for manufacturing titanium alloy wire with enhanced properties
PCT/US2005/018492 WO2006022951A2 (en) 2004-07-22 2005-05-25 Method for manufacturing titanium alloy wire with enhanced properties

Publications (3)

Publication Number Publication Date
EP1784269A2 EP1784269A2 (en) 2007-05-16
EP1784269A4 EP1784269A4 (en) 2008-03-05
EP1784269B1 true EP1784269B1 (en) 2011-12-14

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US (1) US20060016521A1 (en)
EP (1) EP1784269B1 (en)
JP (1) JP5037340B2 (en)
KR (1) KR101184464B1 (en)
CN (1) CN101068945B (en)
ES (1) ES2385086T3 (en)
WO (1) WO2006022951A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107214474A (en) * 2017-05-22 2017-09-29 西部超导材料科技股份有限公司 A kind of preparation method of high-strength Ti6Al7Nb titanium alloy wire materials

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050211475A1 (en) * 2004-04-28 2005-09-29 Mirchandani Prakash K Earth-boring bits
US20080101977A1 (en) * 2005-04-28 2008-05-01 Eason Jimmy W Sintered bodies for earth-boring rotary drill bits and methods of forming the same
US9428822B2 (en) 2004-04-28 2016-08-30 Baker Hughes Incorporated Earth-boring tools and components thereof including material having hard phase in a metallic binder, and metallic binder compositions for use in forming such tools and components
US20060024140A1 (en) * 2004-07-30 2006-02-02 Wolff Edward C Removable tap chasers and tap systems including the same
US7513320B2 (en) * 2004-12-16 2009-04-07 Tdy Industries, Inc. Cemented carbide inserts for earth-boring bits
US8637127B2 (en) 2005-06-27 2014-01-28 Kennametal Inc. Composite article with coolant channels and tool fabrication method
US7687156B2 (en) 2005-08-18 2010-03-30 Tdy Industries, Inc. Composite cutting inserts and methods of making the same
US7597159B2 (en) * 2005-09-09 2009-10-06 Baker Hughes Incorporated Drill bits and drilling tools including abrasive wear-resistant materials
US8002052B2 (en) 2005-09-09 2011-08-23 Baker Hughes Incorporated Particle-matrix composite drill bits with hardfacing
US7776256B2 (en) 2005-11-10 2010-08-17 Baker Huges Incorporated Earth-boring rotary drill bits and methods of manufacturing earth-boring rotary drill bits having particle-matrix composite bit bodies
US7997359B2 (en) 2005-09-09 2011-08-16 Baker Hughes Incorporated Abrasive wear-resistant hardfacing materials, drill bits and drilling tools including abrasive wear-resistant hardfacing materials
US7703555B2 (en) 2005-09-09 2010-04-27 Baker Hughes Incorporated Drilling tools having hardfacing with nickel-based matrix materials and hard particles
US7802495B2 (en) * 2005-11-10 2010-09-28 Baker Hughes Incorporated Methods of forming earth-boring rotary drill bits
US7913779B2 (en) * 2005-11-10 2011-03-29 Baker Hughes Incorporated Earth-boring rotary drill bits including bit bodies having boron carbide particles in aluminum or aluminum-based alloy matrix materials, and methods for forming such bits
US7784567B2 (en) * 2005-11-10 2010-08-31 Baker Hughes Incorporated Earth-boring rotary drill bits including bit bodies comprising reinforced titanium or titanium-based alloy matrix materials, and methods for forming such bits
US7807099B2 (en) 2005-11-10 2010-10-05 Baker Hughes Incorporated Method for forming earth-boring tools comprising silicon carbide composite materials
US8770324B2 (en) * 2008-06-10 2014-07-08 Baker Hughes Incorporated Earth-boring tools including sinterbonded components and partially formed tools configured to be sinterbonded
WO2007127680A1 (en) * 2006-04-27 2007-11-08 Tdy Industries, Inc. Modular fixed cutter earth-boring bits, modular fixed cutter earth-boring bit bodies, and related methods
EP2066864A1 (en) 2006-08-30 2009-06-10 Baker Hughes Incorporated Methods for applying wear-resistant material to exterior surfaces of earth-boring tools and resulting structures
CA2663519A1 (en) 2006-10-25 2008-05-02 Tdy Industries, Inc. Articles having improved resistance to thermal cracking
US7775287B2 (en) * 2006-12-12 2010-08-17 Baker Hughes Incorporated Methods of attaching a shank to a body of an earth-boring drilling tool, and tools formed by such methods
US7841259B2 (en) * 2006-12-27 2010-11-30 Baker Hughes Incorporated Methods of forming bit bodies
US7846551B2 (en) 2007-03-16 2010-12-07 Tdy Industries, Inc. Composite articles
WO2009149071A2 (en) * 2008-06-02 2009-12-10 Tdy Industries, Inc. Cemented carbide-metallic alloy composites
US8790439B2 (en) 2008-06-02 2014-07-29 Kennametal Inc. Composite sintered powder metal articles
US7703556B2 (en) 2008-06-04 2010-04-27 Baker Hughes Incorporated Methods of attaching a shank to a body of an earth-boring tool including a load-bearing joint and tools formed by such methods
US8261632B2 (en) 2008-07-09 2012-09-11 Baker Hughes Incorporated Methods of forming earth-boring drill bits
US8322465B2 (en) 2008-08-22 2012-12-04 TDY Industries, LLC Earth-boring bit parts including hybrid cemented carbides and methods of making the same
US8025112B2 (en) 2008-08-22 2011-09-27 Tdy Industries, Inc. Earth-boring bits and other parts including cemented carbide
US8272816B2 (en) 2009-05-12 2012-09-25 TDY Industries, LLC Composite cemented carbide rotary cutting tools and rotary cutting tool blanks
US8201610B2 (en) 2009-06-05 2012-06-19 Baker Hughes Incorporated Methods for manufacturing downhole tools and downhole tool parts
US8308096B2 (en) 2009-07-14 2012-11-13 TDY Industries, LLC Reinforced roll and method of making same
US9643236B2 (en) * 2009-11-11 2017-05-09 Landis Solutions Llc Thread rolling die and method of making same
MX340467B (en) 2010-05-20 2016-07-08 Baker Hughes Incorporated * Methods of forming at least a portion of earth-boring tools, and articles formed by such methods.
US8490674B2 (en) 2010-05-20 2013-07-23 Baker Hughes Incorporated Methods of forming at least a portion of earth-boring tools
RU2012155100A (en) 2010-05-20 2014-06-27 Бейкер Хьюз Инкорпорейтед METHOD FOR FORMING A LESS PART OF A DRILLING TOOL AND FORMED PRODUCT THEREOF
US20120118433A1 (en) * 2010-11-12 2012-05-17 Fmw Composite Systems, Inc. Method of modifying thermal and electrical properties of multi-component titanium alloys
US8800848B2 (en) 2011-08-31 2014-08-12 Kennametal Inc. Methods of forming wear resistant layers on metallic surfaces
US9016406B2 (en) 2011-09-22 2015-04-28 Kennametal Inc. Cutting inserts for earth-boring bits
CN102634746B (en) * 2012-05-07 2013-12-11 东莞市闻誉实业有限公司 Manufacturing method for enhanced type aluminum, titanium and carbon alloy wire
CN102649222B (en) * 2012-05-31 2014-01-29 浙江振兴石化机械有限公司 Method for processing spindly shaft by utilizing 17-4PH stainless steel
CN102851541B (en) * 2012-09-27 2014-06-18 南京航空航天大学 TiC particle-reinforced titanium-aluminum-molybdenum-silicon alloy material synthesized in situ and preparation method thereof
CN102851537B (en) * 2012-09-27 2014-04-02 南京航空航天大学 In-situ synthesis TiC particle enhanced titanium-aluminum-molybdenum-palladium alloy material and method for preparing same
CN108950302B (en) * 2018-08-03 2019-08-02 中鼎特金秦皇岛科技股份有限公司 A kind of high-strength corrosion-resistant erosion titanium alloy and preparation method thereof
CN111849600B (en) * 2020-08-05 2022-06-07 陕西高精尖新材料科技有限责任公司 Titanium alloy wire high-temperature drawing dry-type lubricant and preparation method thereof

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3343998A (en) * 1964-01-06 1967-09-26 Whittaker Corp High strength wrought weldable titanium alloy mill product manufacture
US3698863A (en) * 1970-01-29 1972-10-17 Brunswick Corp Fibrous metal filaments
US4639281A (en) * 1982-02-19 1987-01-27 Mcdonnell Douglas Corporation Advanced titanium composite
US4499156A (en) * 1983-03-22 1985-02-12 The United States Of America As Represented By The Secretary Of The Air Force Titanium metal-matrix composites
US4631092A (en) * 1984-10-18 1986-12-23 The Garrett Corporation Method for heat treating cast titanium articles to improve their mechanical properties
JPS61159540A (en) * 1985-01-07 1986-07-19 Nippon Gakki Seizo Kk Manufacture of fiber reinforced metallic material
US4731115A (en) * 1985-02-22 1988-03-15 Dynamet Technology Inc. Titanium carbide/titanium alloy composite and process for powder metal cladding
US4714587A (en) * 1987-02-11 1987-12-22 The United States Of America As Represented By The Secretary Of The Air Force Method for producing very fine microstructures in titanium alloy powder compacts
US4968348A (en) * 1988-07-29 1990-11-06 Dynamet Technology, Inc. Titanium diboride/titanium alloy metal matrix microcomposite material and process for powder metal cladding
US4906430A (en) * 1988-07-29 1990-03-06 Dynamet Technology Inc. Titanium diboride/titanium alloy metal matrix microcomposite material and process for powder metal cladding
US5068003A (en) * 1988-11-10 1991-11-26 Sumitomo Metal Industries, Ltd. Wear-resistant titanium alloy and articles made thereof
US4931253A (en) * 1989-08-07 1990-06-05 United States Of America As Represented By The Secretary Of The Air Force Method for producing alpha titanium alloy pm articles
JPH0670263B2 (en) * 1990-01-30 1994-09-07 鈴木金属工業株式会社 High strength titanium wire
JPH0436445A (en) * 1990-05-31 1992-02-06 Sumitomo Metal Ind Ltd Production of corrosion resisting seamless titanium alloy tube
EP0484931B1 (en) * 1990-11-09 1998-01-14 Kabushiki Kaisha Toyota Chuo Kenkyusho Sintered powdered titanium alloy and method for producing the same
US5030277A (en) * 1990-12-17 1991-07-09 The United States Of America As Represented By The Secretary Of The Air Force Method and titanium aluminide matrix composite
JPH04279212A (en) * 1991-03-07 1992-10-05 Shinko Kosen Kogyo Kk Manufacture of fine wire of titanium or its alloys
US5372775A (en) * 1991-08-22 1994-12-13 Sumitomo Electric Industries, Ltd. Method of preparing particle composite alloy having an aluminum matrix
US5366570A (en) * 1993-03-02 1994-11-22 Cermics Venture International Titanium matrix composites
JPH06306508A (en) * 1993-04-22 1994-11-01 Nippon Steel Corp Production of low anisotropy and high fatigue strength titanium base composite material
US5799238A (en) * 1995-06-14 1998-08-25 The United States Of America As Represented By The United States Department Of Energy Method of making multilayered titanium ceramic composites
JPH09256080A (en) * 1996-03-21 1997-09-30 Honda Motor Co Ltd Sintered friction material made of titanium or/and titanium alloy
US5722037A (en) * 1996-05-09 1998-02-24 Korea Institute Of Machinery & Materials Process for producing Ti/TiC composite by hydrocarbon gas and Ti powder reaction
JP2852414B2 (en) * 1996-06-13 1999-02-03 科学技術庁金属材料技術研究所長 Particle-reinforced titanium-based composite material and method for producing the same
US5897830A (en) * 1996-12-06 1999-04-27 Dynamet Technology P/M titanium composite casting
US5903813A (en) * 1998-07-24 1999-05-11 Advanced Materials Products, Inc. Method of forming thin dense metal sections from reactive alloy powders
US6042780A (en) * 1998-12-15 2000-03-28 Huang; Xiaodi Method for manufacturing high performance components
US6190473B1 (en) * 1999-08-12 2001-02-20 The Boenig Company Titanium alloy having enhanced notch toughness and method of producing same
US6402859B1 (en) * 1999-09-10 2002-06-11 Terumo Corporation β-titanium alloy wire, method for its production and medical instruments made by said β-titanium alloy wire
JP4123937B2 (en) * 2001-03-26 2008-07-23 株式会社豊田中央研究所 High strength titanium alloy and method for producing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107214474A (en) * 2017-05-22 2017-09-29 西部超导材料科技股份有限公司 A kind of preparation method of high-strength Ti6Al7Nb titanium alloy wire materials

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