WO1999013117A1 - Copper based alloy featuring precipitation hardening and solid-solution hardening - Google Patents
Copper based alloy featuring precipitation hardening and solid-solution hardening Download PDFInfo
- Publication number
- WO1999013117A1 WO1999013117A1 PCT/US1998/017196 US9817196W WO9913117A1 WO 1999013117 A1 WO1999013117 A1 WO 1999013117A1 US 9817196 W US9817196 W US 9817196W WO 9913117 A1 WO9913117 A1 WO 9913117A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alloy
- content
- hardening
- strength
- copper
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/02—Alloys based on copper with tin as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/06—Alloys based on copper with nickel or cobalt as the next major constituent
Definitions
- This invention relates to a copper alloy, particularly a copper alloy that is especially useful in electrical and electronic interconnection components and switch applications, including high temperature switching. This alloy shows special promise in "spring type” applications.
- U.S. Patent No. 5,041,176 discloses a copper alloy including from 0.1-10% nickel (Ni) ; 0.1-10% tin (Sn) ; 0.05-5% silicon (Si); 0.01-5% iron (Fe) ; and 0.0001-1% boron (B) , by weight.
- This disclosure requires formation of an Ni-Si intermetallic compound homogeneously dispersed in the alloy. Fe is required for age hardening. However, at Fe concentrations greater than 5%, electrical conductivity is compromised and corrosion becomes a serious problem.
- B is incorporated into the alloy to improve corrosion resistance, hardness and strength. High hardness is achieved by precipitation hardening at a tempering temperature of 400° to 450°C. Si also serves as a deoxidizer.
- the Mikawa alloy is suitable for use in electronic parts where good electrical conductivity, heat conductivity, strength, hardness, plating ability, soldering ability, elasticity, and corrosion resistance including resistance to acids are required, this alloy is of a different composition and displays different characteristics from those obtainable according to the instant invention.
- Kubosono et al . Another comparison alloy is disclosed by Kubosono et al . , U.S. Patent No. 5,516,484.
- Kubosono et al . discloses copper- nickel based alloys that are processed using horizontal continuous casting with a graphite mold.
- the Ni-Cu alloy system is essentially a different alloy than the alloy of the instant invention.
- copper (Cu) is an undesired impurity whose content must be kept below 0.02%.
- Kubosono et al . teaches that effects obtainable by addition of Si cannot be recognized if no B s present.
- U.S. Patent No. 5,334,346 to Ki et al . discloses a high performance copper alloy for electrical and electronic parts.
- the Kim alloy consists essentially of copper and 0.5 to 2.4% by weight Ni ; 0.1-0.5% Si; 0.02 to 0.16% P; and 0.02 to 0.2% magnesium (Mg) .
- Kim et al discusses precipitation hardening where N ⁇ 2 S ⁇ and N ⁇ 3 P precipitate in the copper matrix. Any excess of free Si and P, is taught as causing formation of brittle intermetallic compounds which lead to peeling and cracking.
- Mg is proposed as a scavenger element to remove free Si and P. However, as content of Mg increases, conductivity and utility of the alloy are compromised. Zinc (Zn) and Fe are also disclosed as possible scavengers. This alloy does not contain Sn.
- Hashizume et al . U.S. Patent No. 5,064,611 discloses a process for producing a copper alloy that contains 1-8% Ni ; 0.1-0.8% P; 0.6-1.0% Si; optionally, 0.03 to 0.5% Zn; and Cu.
- N ⁇ 5 P 2 and N ⁇ 2 S ⁇ are disclosed as intermetallic compounds for increasing mechanical strength of the alloy with minimal decrease m electrical conductivity. Sn is not present m this alloy.
- a copper-tm alloy i.e., bronze, Asai et al . , U.S. Patent No.
- 5,021,105 discloses an alloy comprising 2.0-7.0% Sn; 1.0-6.0% Ni , cobalt (Co) or chromium (Cr) ; 0.1-2.0% Si; and Cu.
- This alloy may be processed to exhibit elongation of 3-20%; strength of 70-100 kg/mm 2 ; and electroconductivity from 10-30% IACS .
- Ni is disclosed as being important for strengthening; Cr is disclosed as improving hot rolling properties and heat resistance; and Co is disclosed as contributing to effective heat resistance.
- Sn content is limited to 7% by the hot rolling method used to process the alloy.
- Asai et al . does not disclose phosphorus (P) as a constituent.
- Arita et al . U.S. Patent No. 4,337,089, discloses a Cu-Ni-Sn alloy containing 0.5-3.0% Ni; 0.3-0.9% Sn; 0.01-0.2% P; 0.0-0.35% manganese (Mn) or Si; and Cu.
- This alloy features 60 kg/mm 2 tensile strength and elongation of more than 6% (i.e., to provide the mechanical property necessary for bend working) by combining heat treatment and cold rolling in its processing.
- Si or Mn is incorporated to enhance strength.
- the low Sn content disclosed m Arita et al . does not provide the combined formability-strength properties of the instant invention.
- U.S. Patent No. 5,132,083 teaches a laser padding material which is a powder containing 1-5% Ni ; 0.2-5% Si; less than 1% B; less than 2% P; less than 3% Mn; and Cu. Sn and lead (Pb) are optional ingredients, at 8-15% for each.
- This powder can be laser processed to produce a copper laser padding material excellent in slidmg-abrasion resistance.
- the chemistries involved n laser padding are not the same as m the alloy of the instant invention. For example, no rolling, hot or cold, is used to process the padding material.
- a designation system for providing a means for defining and identifying coppers and copper alloys is known as UNS
- Th s system is in common use m
- UNS alloy C85800 is a leaded yellow brass containing 1.5% Sn, 1.5% Pb, 31-41% Zn, 0.5% Fe, 0.05%Sb, 0.5% Ni (inci Co), 0.25% Mn, 0.05% As, 0.05% S, 0.01% P, 0.55% Al , 0.25% Si and 57.0% minimum Cu.
- the present invention provides a phosphor bronze alloy with characteristics much improved over those known in the art.
- the invention provides an alloy that when processed has desired spring and strength properties and superior durability especially at higher temperatures at an economic price.
- Figure 1 depicts softening behavior data curves for alloy MHP101 of the Example and of comparative alloys.
- Figure 2 depicts stress relaxation data curves for alloy MHP101 of the Example and of comparative alloys.
- a particle dispersion enhanced phosphor bronze in accordance with the present invention includes a nickel content of from 0.4 to 3.0% by weight; a Si content of from 0.1 to 1.0% by weight; a P content of from 0.01-0.35% by weight; a Sn content of 1.0-11.0% by weight and copper.
- Sn enhances formability at a given level of strength.
- P helps impart optimal spring and strength properties as well as providing fluidity in casting copper based alloys.
- P also aids in deoxidation of the melt.
- P is the primary deoxidizer of the melt. Si is not lost in uncontrolled quantities in the melting process, which permits maintaining a stoichiometrical relationship between Si and Ni in the alloy.
- Sn content of below 8% and P content of 0.01-0.2% by wt . are especially preferred in some embodiments.
- Solid solution hardening is contributed by tin, phosphorous and copper, while precipitation hardening resides in nickel silicide and nickel phosphides precipitated in the matrix.
- Solid solution of a copper base occurs when the alloying element is dissolved to form a homogenous liquid solution. When the solution is frozen and subsequently rolled/annealed, the alloying metal goes into solution to form a solid solution. The alloying element thereby becomes an integral part of the matrix crystal .
- Substitution of elements in solid solution tends to increase the strength of the metal as it decreases electrical conductivity.
- the increased strength is related to a greater resistance to slip.
- the solute atoms are different in size from the copper atoms, causing a distortion of the lattice structure that imparts slip resistance. That is, greater energy is required to distort the lattice.
- the phosphor bronze according to the instant invention has consistent mechanical properties, optimum yield strength and excellent formability.
- the alloy is especially useful in high temperature applications, e.g., where operational temperatures may reach 140°C, 150°C or higher, for example, up to 200°C in specific applications.
- the alloy is designed to be a high strength alloy with moderate conductivity. In these applications, no comparable alloy has been previously available.
- the alloy family will have the strength and formability of known phosphor bronzes, but will exhibit superior resistance to stress relaxation especially at elevated temperatures .
- the material for the alloy is mixed according to desired concentrations and melted in channel or coreless electric induction furnaces.
- the obtained melt is horizontally continuous cast through a graphite die.
- This process is sometimes referred to as horizontal thin strip continuous casting.
- Special enhanced cooling can be employed to assure proper quenching of solidified material, to maintain all solute in solution.
- the preferred casting practice employs special enhanced cooling within the graphite die assembly to assure a sufficiently rapid quench of the just-solidified metal from its solidus temperature to a temperature below 450°C. This assures that the solute remains to a high degree (estimated at approx. 90%) in solution, and does not have time to significantly precipitate during the cooling phase.
- This enhanced cooling involves the use of high thermal conductivity (minimum .77 cal/cm/sec) copper plates to which a high thermal conductivity graphite die (minimum .29 cal/cm/sec) has been bolted as per current standard art.
- the invention introduces a high conductivity gas such as Helium or Hydrogen or mixtures thereof, or carrier gases with significant concentrations of Helium and/or Hydrogen, between the copper plates and graphite plates of the assembly.
- the high conductivity gas replaces atmospheric 0 2 /N 2 in the copper/graphite interface, thereby improving the cooling action.
- the cast material is surface milled and then rolled down to thinner gages. Heat treatments are imposed in the course of rolling to assure 1) maximum solution of alloying elements, and 2) precipitation of the dissolved alloying elements.
- the precipitate provides strength and resistance to stress relaxation. Less cold rolling is required to achieve the same tensile strength as Sn concentration (solid solution content) of the alloy increases. Less cold rolling permits more subsequent forming operations.
- the material is for some applications further rolled to attain increased strength, and may or may not be stress relieved thermally and/or mechanically at finish.
- improved solutioning of the solute is obtained by heat treating at elevated temperatures at the cast stage, or at intermediate stages .
- the process stages in accordance with the instant invention can include the following protocols: One embodiment (for those mills so equipped)
- the homogenization assures maximum solutioning of alloying elements.
- the quench assures maximum solution is retained. Temperature attained is 800-950°C.
- Roll Rapid anneal with quench may need multiple "anneal with quench” steps in process to reach light gages
- Rapid anneal with quench may need multiple "anneal with quench” steps in process to reach light gages)
- the invention overcomes problems previously plaguing the art wherein hot rolling technologies did not permit P to be used at levels as instantly claimed. Also the instant invention provides an alloy that can contain if desired, a wide range of Sn content, for example, greater than 7% Sn,
- Sn content be 8% by weight or less, for example, 7%, 5%, and possibly approaching 3%.
- Sn content may prove advantageous due to its high electrical conductivity and moderate strength. Alloys with Sn content below 1% will have lower potential strength levels and will not achieve the contact forces required in some more demanding spring contact applications .
- P levels of 0.01-0.20 may prove particularly advantageous in many applications.
- Ni and Si in the phosphor bronze according to the invention allow improved strengths and will increase the alloy' s resistance to stress relaxation at elevated temperatures where the alloy may be used.
- the instant invention provides a metal alloy comprising by weight : Sn 1.0-11.0% Ni 0.4-3.0% Si 0.1-1.0% P 0.01-0.35% Cu comprises the balance.
- Preferred embodiments of this invention may be limited to preferred subranges of various components, e.g., Sn content of below 8%, 1.0 to 1.5%, 2.1 to 2.7%, 4.7-5.3%, 1-7%, 7-11%, 7-8% or 7-9%, etc.
- other constituents such as P may be preferably limited to, for example, 0.01-0.2%, 0.01 to 0.06%, 0.05-0.18 or 0.2, etc.
- Si content can be 0.22-0.30% or 0.4-0.5%.
- Ni content can be 1.3- 1.7%, 2.5-3.0%, or 1.0-3.0%, etc.
- this alloy consists essentially of, by weight:
- the inventive alloy consists essentially of :
- the alloy consists of, by weight:
- the alloys according to the instantly claimed invention will demonstrate improved properties, for example, conductivity and tensile strength, over those alloys known in the art. Devices incorporating the alloy will be more economical to produce and maintain and will demonstrate improved durability.
- Table 1 shows a comparison of exemplary alloys according to the invention, with several standard phosphor bronze alloys.
- an alloy designated alloy MHPlOl was cast with the chemistry as follows :
- the material was processed to .0070" thick and had mechanical properties as follows in the bare conditions unless otherwise stated:
- the softening behavior is shown in Figure 1 compared with data of C51100 alloy (4% Sn Phosphor Bronze) and C52100 (8% Sn Phosphor Bronze) .
- the time at temperature was one hour.
- the stress relaxation behavior is shown in Figure 2 compared with C51100 alloy.
- the test stress was 80% of initial stress, and the initial stress in the test sample was 88ksi.
- the test temperature was 150°C.
- Expected electronic application guide data for MHPlOl and other alloys according to the instant invention compared to similar UNS designated alloys are shown in Table 1.
- MHP is a trademark of The Miller Company, the assignee of the invention of the subject patent application.
- the data collected for MHPlOl confirm that alloy formulations of the instant invention provide resistance to stress relaxation at higher temperatures than the current offering to standard Phosphor Bronze alloys such as the C51100 used in the comparison.
- strengths equal to higher tin-containing Phosphor Bronzes can be achieved with increased electrical conductivity.
- the alloy MHPlOl an example of the alloys of the instant invention, is thus shown to have excellent formability properties.
- the invention also provides the above described alloy for use as a casting material.
- the invention also includes embodiments for certain applications that may demand smaller ranges of constituents, e.g., 0.02-0.2% P, than described above. All subranges within the above-described ranges are contemplated as part of the invention.
- Sn over 7% for example, nominal Sn content of 8%, 9%, or 10% will add strength to the alloy.
- the alloy will also have better formability at a given tensile strength.
- the invention especially includes embodiments where the alloy displays properties of solid solution hardening, and precipitation hardening, and dispersion hardening.
- Another aspect of the invention is a phosphor bronze casting.
- the product resulting from the processing of the casting is useful as a material for electrical lead conductor applications.
- Such applications include those relating to integrated circuits and those encountered in the automotive industry such as engine compartment circuitry.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Conductive Materials (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Claims
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE69814657T DE69814657T2 (en) | 1997-09-05 | 1998-08-21 | COPPER BASED ALLOY, CHARACTERIZED BY DECAY CURING AND CURING IN SOLID CONDITION |
| AU91083/98A AU9108398A (en) | 1997-09-05 | 1998-08-21 | Copper based alloy featuring precipitation hardening and solid-solution hardening |
| US09/486,969 US6379478B1 (en) | 1998-08-21 | 1998-08-21 | Copper based alloy featuring precipitation hardening and solid-solution hardening |
| AT98943252T ATE240413T1 (en) | 1997-09-05 | 1998-08-21 | COPPER-BASED ALLOY CHARACTERIZED BY PRECIPITATION HARDENING AND SOLID STATE HARDENING |
| CA002303164A CA2303164A1 (en) | 1997-09-05 | 1998-08-21 | Copper based alloy featuring precipitation hardening and solid-solution hardening |
| BR9811448-4A BR9811448A (en) | 1997-09-05 | 1998-08-21 | Copper based alloy depicting precipitation quenching and solid solution quenching |
| JP2000510901A JP2001515960A (en) | 1997-09-05 | 1998-08-21 | Copper-based alloy characterized by precipitation hardening and solid solution hardening |
| EP98943252A EP1021575B1 (en) | 1997-09-05 | 1998-08-21 | Copper based alloy featuring precipitation hardening and solid-solution hardening |
| KR1020007002353A KR20010023699A (en) | 1997-09-05 | 1998-08-21 | Copper based alloy featuring precipitation hardening and solid-solution hardening |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5777997P | 1997-09-05 | 1997-09-05 | |
| US60/057,779 | 1997-09-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1999013117A1 true WO1999013117A1 (en) | 1999-03-18 |
Family
ID=22012718
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1998/017196 Ceased WO1999013117A1 (en) | 1997-09-05 | 1998-08-21 | Copper based alloy featuring precipitation hardening and solid-solution hardening |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP1021575B1 (en) |
| JP (1) | JP2001515960A (en) |
| KR (1) | KR20010023699A (en) |
| CN (1) | CN1097095C (en) |
| AR (1) | AR017044A1 (en) |
| AT (1) | ATE240413T1 (en) |
| AU (1) | AU9108398A (en) |
| BR (1) | BR9811448A (en) |
| CA (1) | CA2303164A1 (en) |
| DE (1) | DE69814657T2 (en) |
| TW (1) | TW364019B (en) |
| WO (1) | WO1999013117A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7163753B2 (en) | 2002-04-15 | 2007-01-16 | Sumitomo Wiring Systems, Ltd. | Arc-resistant terminal, arc-resistant terminal couple and connector or the like for automobile |
| EP2048251A4 (en) * | 2006-05-26 | 2009-10-14 | Kobe Steel Ltd | Copper alloy having high strength, high electric conductivity and excellent bending workability |
| US20220126363A1 (en) * | 2019-02-07 | 2022-04-28 | Equispheres Inc., | Alloys with a low density of precipitates for use in applications that include remelting processes, and preparation process thereof |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4100629B2 (en) * | 2004-04-16 | 2008-06-11 | 日鉱金属株式会社 | High strength and high conductivity copper alloy |
| WO2009098810A1 (en) * | 2008-02-08 | 2009-08-13 | Mitsui Mining & Smelting Co., Ltd. | Process for producing precipitation-hardened copper alloy strip |
| JP5492089B2 (en) * | 2008-09-10 | 2014-05-14 | 大豊工業株式会社 | Pb-free Cu-Bi sintered material sliding parts |
| CN106435250A (en) * | 2009-04-08 | 2017-02-22 | 瑞士金属-Ums瑞士金属加工有限公司 | Machinable copper base alloy and production method thereof |
| KR102107585B1 (en) * | 2019-11-22 | 2020-05-07 | 주식회사 풍산 | Copper alloy material with excellent wear resistance and method for producing same |
| CN110923505B (en) * | 2019-12-31 | 2021-11-02 | 内蒙古工业大学 | Cu-Ni-Mn alloy and its preparation method and application |
| CN113249612A (en) * | 2021-04-21 | 2021-08-13 | 铁岭富兴铜业有限公司 | Novel contact copper alloy and preparation method thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU219368A1 (en) * | 1966-07-16 | 1968-05-30 | Припой Пайки Меди | |
| US4337089A (en) * | 1980-07-25 | 1982-06-29 | Nippon Telegraph And Telephone Public Corporation | Copper-nickel-tin alloys for lead conductor materials for integrated circuits and a method for producing the same |
| JPH02197543A (en) * | 1989-01-26 | 1990-08-06 | Furukawa Electric Co Ltd:The | Copper alloy for connecting apparatus |
| US4971758A (en) * | 1989-07-25 | 1990-11-20 | Mitsubishi Shindoh Co., Ltd. | Copper-based alloy connector for electrical devices |
| DE4338769A1 (en) * | 1992-11-13 | 1994-05-19 | Mitsubishi Shindo Kk | Copper@ alloy for use in mfr. of electrical components - contg. nickel@, tin@, silicon@, zinc@, iron@, phosphorus@, and magnesium@ |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61143564A (en) * | 1984-12-13 | 1986-07-01 | Nippon Mining Co Ltd | Manufacturing method of high strength and high conductivity copper-based alloy |
| JPH02122039A (en) * | 1988-10-31 | 1990-05-09 | Nippon Mining Co Ltd | High-strength, high-conductivity copper alloy with excellent oxide film adhesion |
-
1998
- 1998-08-21 AU AU91083/98A patent/AU9108398A/en not_active Abandoned
- 1998-08-21 EP EP98943252A patent/EP1021575B1/en not_active Expired - Lifetime
- 1998-08-21 BR BR9811448-4A patent/BR9811448A/en not_active Application Discontinuation
- 1998-08-21 WO PCT/US1998/017196 patent/WO1999013117A1/en not_active Ceased
- 1998-08-21 KR KR1020007002353A patent/KR20010023699A/en not_active Withdrawn
- 1998-08-21 CA CA002303164A patent/CA2303164A1/en not_active Abandoned
- 1998-08-21 DE DE69814657T patent/DE69814657T2/en not_active Expired - Fee Related
- 1998-08-21 CN CN98810040A patent/CN1097095C/en not_active Expired - Fee Related
- 1998-08-21 AT AT98943252T patent/ATE240413T1/en not_active IP Right Cessation
- 1998-08-21 JP JP2000510901A patent/JP2001515960A/en not_active Withdrawn
- 1998-08-27 TW TW087114229A patent/TW364019B/en active
- 1998-09-01 AR ARP980104367A patent/AR017044A1/en unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU219368A1 (en) * | 1966-07-16 | 1968-05-30 | Припой Пайки Меди | |
| US4337089A (en) * | 1980-07-25 | 1982-06-29 | Nippon Telegraph And Telephone Public Corporation | Copper-nickel-tin alloys for lead conductor materials for integrated circuits and a method for producing the same |
| JPH02197543A (en) * | 1989-01-26 | 1990-08-06 | Furukawa Electric Co Ltd:The | Copper alloy for connecting apparatus |
| US4971758A (en) * | 1989-07-25 | 1990-11-20 | Mitsubishi Shindoh Co., Ltd. | Copper-based alloy connector for electrical devices |
| DE4338769A1 (en) * | 1992-11-13 | 1994-05-19 | Mitsubishi Shindo Kk | Copper@ alloy for use in mfr. of electrical components - contg. nickel@, tin@, silicon@, zinc@, iron@, phosphorus@, and magnesium@ |
Non-Patent Citations (1)
| Title |
|---|
| PATENT ABSTRACTS OF JAPAN vol. 14, no. 480 (C - 771) 19 October 1990 (1990-10-19) * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7163753B2 (en) | 2002-04-15 | 2007-01-16 | Sumitomo Wiring Systems, Ltd. | Arc-resistant terminal, arc-resistant terminal couple and connector or the like for automobile |
| EP2048251A4 (en) * | 2006-05-26 | 2009-10-14 | Kobe Steel Ltd | Copper alloy having high strength, high electric conductivity and excellent bending workability |
| US8268098B2 (en) | 2006-05-26 | 2012-09-18 | Kobe Steel, Ltd. | Copper alloy having high strength, high electric conductivity and excellent bending workability |
| US8357248B2 (en) | 2006-05-26 | 2013-01-22 | Kobe Steel, Ltd. | Copper alloy having high strength, high electric conductivity and excellent bending workability |
| US9177686B2 (en) | 2006-05-26 | 2015-11-03 | Kobe Steel, Ltd. | Copper alloy having high strength, high electric conductivity and excellent bending workability |
| US20220126363A1 (en) * | 2019-02-07 | 2022-04-28 | Equispheres Inc., | Alloys with a low density of precipitates for use in applications that include remelting processes, and preparation process thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| BR9811448A (en) | 2000-08-22 |
| CN1097095C (en) | 2002-12-25 |
| DE69814657D1 (en) | 2003-06-18 |
| EP1021575B1 (en) | 2003-05-14 |
| TW364019B (en) | 1999-07-11 |
| AR017044A1 (en) | 2001-08-22 |
| CN1275171A (en) | 2000-11-29 |
| EP1021575A1 (en) | 2000-07-26 |
| ATE240413T1 (en) | 2003-05-15 |
| DE69814657T2 (en) | 2004-03-25 |
| JP2001515960A (en) | 2001-09-25 |
| CA2303164A1 (en) | 1999-03-18 |
| KR20010023699A (en) | 2001-03-26 |
| AU9108398A (en) | 1999-03-29 |
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