EP2695957B1 - Kupferlegierungsblech - Google Patents
Kupferlegierungsblech Download PDFInfo
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- EP2695957B1 EP2695957B1 EP13005148.5A EP13005148A EP2695957B1 EP 2695957 B1 EP2695957 B1 EP 2695957B1 EP 13005148 A EP13005148 A EP 13005148A EP 2695957 B1 EP2695957 B1 EP 2695957B1
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- EP
- European Patent Office
- Prior art keywords
- copper alloy
- sheet
- less
- stress relaxation
- alloy sheet
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- 229910000881 Cu alloy Inorganic materials 0.000 title claims description 112
- 238000002441 X-ray diffraction Methods 0.000 claims description 42
- 239000010949 copper Substances 0.000 claims description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 11
- 229910052802 copper Inorganic materials 0.000 claims description 11
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 7
- 229910052719 titanium Inorganic materials 0.000 claims description 7
- 229910052726 zirconium Inorganic materials 0.000 claims description 7
- 229910052790 beryllium Inorganic materials 0.000 claims description 6
- 229910052793 cadmium Inorganic materials 0.000 claims description 6
- 229910052737 gold Inorganic materials 0.000 claims description 6
- 229910052697 platinum Inorganic materials 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 6
- 229910001122 Mischmetal Inorganic materials 0.000 claims description 5
- 229910052776 Thorium Inorganic materials 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 229910052787 antimony Inorganic materials 0.000 claims description 5
- 229910052785 arsenic Inorganic materials 0.000 claims description 5
- 229910052797 bismuth Inorganic materials 0.000 claims description 5
- 229910052796 boron Inorganic materials 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 229910052733 gallium Inorganic materials 0.000 claims description 5
- 229910052732 germanium Inorganic materials 0.000 claims description 5
- 229910052735 hafnium Inorganic materials 0.000 claims description 5
- 229910052738 indium Inorganic materials 0.000 claims description 5
- 229910052744 lithium Inorganic materials 0.000 claims description 5
- 229910052758 niobium Inorganic materials 0.000 claims description 5
- 229910052763 palladium Inorganic materials 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 229910052712 strontium Inorganic materials 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 229910052714 tellurium Inorganic materials 0.000 claims description 5
- 229910052721 tungsten Inorganic materials 0.000 claims description 5
- 229910052720 vanadium Inorganic materials 0.000 claims description 5
- 229910052727 yttrium Inorganic materials 0.000 claims description 5
- 229910045601 alloy Inorganic materials 0.000 description 46
- 239000000956 alloy Substances 0.000 description 46
- 238000005096 rolling process Methods 0.000 description 38
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- 238000009825 accumulation Methods 0.000 description 6
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- 229910017824 Cu—Fe—P Inorganic materials 0.000 description 5
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- 238000002844 melting Methods 0.000 description 5
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- 229910052742 iron Inorganic materials 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 238000004873 anchoring Methods 0.000 description 2
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229910017532 Cu-Be Inorganic materials 0.000 description 1
- 229910017876 Cu—Ni—Si Inorganic materials 0.000 description 1
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- 238000000833 X-ray absorption fine structure spectroscopy Methods 0.000 description 1
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Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/02—Contact members
- H01R13/03—Contact members characterised by the material, e.g. plating, or coating materials
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/02—Contact members
- H01R13/10—Sockets for co-operation with pins or blades
- H01R13/11—Resilient sockets
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R43/00—Apparatus or processes specially adapted for manufacturing, assembling, maintaining, or repairing of line connectors or current collectors or for joining electric conductors
- H01R43/16—Apparatus or processes specially adapted for manufacturing, assembling, maintaining, or repairing of line connectors or current collectors or for joining electric conductors for manufacturing contact members, e.g. by punching and by bending
Definitions
- the present invention relates to a cold rolled copper alloy sheet. More specifically, the present invention relates to a copper alloy sheet having properties suitable for a connection component such as automotive terminal or connector.
- connection component such as automotive terminal or connector recently requires a performance enough to ensure reliability in a high-temperature environment such as engine room.
- One of most important properties for the reliability in a high-temperature environment is a contact-fitting force maintaining characteristic, that is, a stress relaxation resistance characteristic.
- Fig. 2 shows a structure of a box-type connector (female terminal 3) representative of a connection component such as automotive terminal or connector.
- Fig. 2(a) is an elevational view and Fig. 2(b) is a cross-sectional view.
- the female terminal 3 has a pressing strip 5 cantilever-supported in an upper holder part 4 and when a male terminal (tab) 6 is inserted into the holder, the pressing strip 5 is elastically deformed and the male terminal (tab) 6 is fixed by the reaction force.
- 7 is a wire connecting part and 8 is an anchoring tongue strip.
- the stress relaxation resistance characteristic is such a resistance characteristic against high temperatures as not allowing great reduction in the contact-fitting force of the spring-shaped component composed of a copper alloy sheet even when the connection component is kept standing in a high-temperature environment.
- Figs. 1(a), and (b) each shows a tester for the stress relaxation resistance characteristic according to this standard. Using this tester, a test specimen 1 cut out into a strip shape is fixed at one end to a rigid test board 2, warped by lifting another end in a cantilever manner (d: warpage size), kept standing at a predetermined temperature for a predetermined time, and then unloaded at room temperature, and the warpage size after unloading (permanent distortion) is determined as ⁇ .
- the stress relaxation ratio of a copper alloy sheet has anisotropy and takes a different value according to the direction in which the longitudinal direction of the test specimen runs with respect to the rolling direction of the copper alloy sheet.
- the connection component such as automotive terminal or connector must have a stress relaxation ratio of 15% or less in the direction used as a spring, that is, in either one direction parallel or orthogonal to the rolling direction of the sheet.
- a Cu-Ni-Si-based alloy, a Cu-Ti-based alloy, a Cu-Be-based alloy and the like have been heretofore widely known, but in recent years, a Cu-Ni-Sn-P-based alloy having a relatively small additive element content has been used.
- This Cu-Ni-Sn-P-based alloy allows for ingot making in a shaft furnace which is a large-scale melting furnace with the opening being widely opened to the atmosphere, and because of its high productivity, a great cost down can be achieved.
- Patent Documents 1 and 2 disclose a technique of uniformly and finely dispersing an Ni-P intermetallic compound in a Cu-Ni-Sn-P-based alloy matrix to enhance the electrical conductivity and at the same time, enhance the stress relaxation resistance characteristic and the like
- Patent Documents 2 and 3 disclose a technique of decreasing the P content of a Cu-Ni-Sn-P-based alloy to obtain a solid solution-type copper alloy reduced in the precipitation of an Ni-P compound.
- Patent Documents 4 and 5 disclose a technique of specifying the substantial temperature and holding time in finish annealing at the production of a Cu-Ni-Sn-P-based alloy sheet to enhance the electrical conductivity and at the same time, enhance the stress relaxation resistance characteristic and the like.
- WO 2006/132317 A1 discloses a Cu-Ni-Sn-P based alloy comprising 0.1 to 3.0 mass% of Ni, 0.01 to 3.0 mass% of Sn, 0.01 to 0.3 mass% of P with the remainder being copper and inevitable impurities.
- EP 1 801 249 A1 discloses a Cu-Ni-Sn-P based alloy comprising 0.1 to 3.0% of Ni, 0.1 to 3.0% of Sn, and 0.01 to 0.3% of P in mass percent respectively, and the remainder being copper and inevitable impurities, wherein in a radial distribution function around a Ni atom according to a XAFS analysis method, a first peak position is within a range of 2.16 to 2.35 ⁇ , the position indicating a distance between a Ni atom in Cu and an atom nearest to the Ni atom.
- EP 1 612 285 A1 discloses a Cu-Ni-Sn-P based alloy containing Ni, Sn, P and also at least one or more elements selected from a group consisting of Zn, Si, Fe, Co, Mg, Ti, Cr, Zr and A1 in a total amount of 0.01-30 wt.% with the remainder being Cu and unavoidable impurities, where the x-ray diffraction intensity ratio of the surface S ND is specified.
- JP 2006 342389 A discloses a copper alloy sheet having a composition which is composed of 0.4 to 1.6% of Ni, 0.4 to 1.6% of Sn, 0.027 to 0.15 of P and 0.005 to 0.15% of Fe in mass percent respectively, and the remainder being copper and inevitable impurities, wherein the ratio of the Ni content and P content is ⁇ 1.5, wherein the copper alloy sheet has a structure in which precipitates of an Ni-P intermetallic compound are dispersed in the matrix phase of the copper alloy and the precipitates have a diameter of ⁇ 60 nm, and ⁇ 20 pieces of the precipitates having a diameter of 5 to 60 nm are observed in the region of a visual field of 500 nm ⁇ 500 nm.
- JP 2001 262297 A also discloses a Cu-Ni-Sn-P based alloy comprising 0.2 to 3.0 mass% of Ni, 2.0 mass% or less of Sn, 0.005 to 2.0 mass% of P with the remainder being copper and inevitable impurities.
- JP 2000 256814 A discloses a Cu-Ni-Sn-P based alloy comprising 0.2 to 3.0 mass% of Ni, 0.5 to 2.0 mass% of Sn, 0.01 to 1.0 mass% of P with the remainder being copper and inevitable impurities.
- JP 2001 262255 A discloses a Cu-Ni-Sn-P based alloy comprising 0.2 to 3.0 mass% of Ni, 2.0 mass% or less of Sn, 0.005 to 2.0 mass% of P with the remainder being copper and inevitable impurities.
- the stress relaxation ratio of a rolled copper alloy sheet (obtained by rolling) has anisotropy and takes a different value according to the direction in which the longitudinal direction of the female terminal 3 in Fig. 2 runs with respect to the rolling direction of the raw material copper alloy sheet.
- the measurement of the stress relaxation ratio and the measured stress relaxation ratio takes a different value according to the direction in which the longitudinal direction of a test specimen runs with respect to the rolling direction of the raw material copper alloy sheet. Accordingly, the stress relaxation ratio is liable to be low in the orthogonal direction than in the parallel direction with respect to the rolling direction of the copper alloy sheet.
- blanking is sometimes performed such that the longitudinal direction of the female terminal 3 (the longitudinal direction of the pressing strip 5) runs in the direction orthogonal to the rolling direction.
- a high stress relaxation resistance characteristic is usually required for the bending (elastic deformation) in the length direction of the pressing strip 5. Accordingly, when blanking is performed to allow for running in the direction orthogonal to the rolling direction, it is required to have a high stress relaxation resistance characteristic not in the parallel direction but in the orthogonal direction with respect to the rolling direction of the copper alloy sheet.
- the stress relaxation resistance characteristic as a terminal or connector can be satisfied irrespective of the blanking direction of the raw material copper alloy sheet.
- the conventional Cu-Ni-Sn-P-based copper alloy enhanced in the stress relaxation resistance characteristic is not excellent in bendability or press punchability.
- the working of a copper alloy sheet into a terminal or connector sometimes involves a severe bending work such as contact bending or 90° bending after notching or a stamping work such as press punching of the sheet, and bendability high enough to withstand such a working or excellent press punchability is becoming required.
- an object of the present invention is to provide a Cu-Ni-Sn-P-based copper alloy sheet which not only satisfies the properties required for a terminal or connector, such as stress relaxation resistance characteristic, but also is excellent in the press punchability.
- the gist of the copper alloy sheet excellent in the stress relaxation resistance characteristic and press punchability is a cold rolled copper alloy sheet consisting of, in terms of mass%, 0.1 to 3.0% of Ni, 0.01 to 3.0% of Sn and 0.01 to 0.3% of P, and optionally at least one member selected from the group consisting of, in terms of mass%, 0.3% or less of Fe, 0.05% or less of Zn, 0.1% or less of Mn, 0.1% or less of Si and 0.3% or less of Mg, optionally at least one member selected from the group consisting of Ca, Zr, Ag, Cr, Cd, Be, Ti, Co, Au and Pt, in a total amount of 1.0 mass% or less, and optionally at least one member selected from the group consisting of Hf, Th, Li, Na, K, Sr, Pd, W, S, C, Nb, Al, V, Y, Mo, Pb, In, Ga
- the dislocation density of the Cu-Ni-Sn-P-based copper alloy sheet texture is controlled. More specifically, the dislocation density of the Cu-Ni-Sn-P-based copper alloy sheet texture is increased, whereby the press punchability is enhanced.
- the amount of dislocations introduced can be controlled by the rolling conditions of the Cu-Ni-Sn-P-based copper alloy and at the same time, this control of the dislocation density has a great effect of enhancing the press punchability.
- the present invention it is not intended to control the crystal orientation texture such as accumulation ratio of a specific orientation (crystal orientation) by specifying the X-ray diffraction intensity from a specific crystal orientation in a sheet surface of a Cu-Fe-P-based copper alloy or the like, which is attempted, for example, in JP-A-2000-328158 , JP-A-2002-339028 , JP-A-2000-328157 and JP-A-2006-63431 .
- a specific orientation crystal orientation
- the dislocation density which is controlled in the embodiment of the present invention is an extremely microscopic issue and it is very difficult to directly observe or quantify the dislocation density introduced into the Cu-Ni-Sn-P-based copper alloy sheet texture.
- the dislocation density introduced into the Cu-Ni-Sn-P-based copper alloy sheet texture is fairly well correlated to the half-value breadth of the X-ray diffraction intensity peak, particularly, the value obtained by dividing the half-value breadth by the height of the X-ray diffraction intensity peak.
- the dislocation density is correlated equally to any X-ray diffraction intensity peak.
- the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface specified in the embodiment of the present invention, is not large (high) as the X-ray diffraction intensity peak which should divide the half-value breadth, in comparison with X-ray diffraction intensities from other planes, and because of a relatively fair half-value breadth, the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak by the height is highly reliable. Accordingly, in the embodiment of the present invention, the dislocation density is indirectly but exactly and reproducibly specified and quantified by the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface.
- the amount of dislocation density is specified by the half-value breadth of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface, which is closely correlated to the amount of dislocation density, to enhance the press punchability and satisfy the press punchability required for the Cu-Ni-Sn-P-based copper alloy sheet.
- the copper alloy sheet is specified to have a dislocation density in not less than a given amount such that the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the Cu-Ni-Sn-P-based copper alloy sheet surface by the peak height is 1.0 ⁇ 10 -4 or more.
- the dislocation density introduced into the sheet is reduced, making a little difference from the conventional Cu-Ni-Sn-P-based with a small dislocation density, and the stress relaxation resistance characteristic and press punchability are decreased or not enhanced.
- the half-value breadth is defined as a width ( ⁇ ) of the X-ray diffraction intensity peak at the position half (height: H/2) the X-ray diffraction intensity peak (height: H) shown in a schematic view of Fig. 3 where the ordinate indicates the X-ray diffraction intensity and the abscissa indicates the angle (2 ⁇ ).
- the half-value breadth of the X-ray diffraction intensity peak is usually used for determining or quantifying the crystallinity or non-crystallinity of metal surface, the crystallite size or the lattice strain.
- the dislocation density that cannot be directly observed or quantified is specified using the value ( ⁇ /H) obtained by dividing the half-value breadth ⁇ of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface, which is fairly well correlated to the dislocation density, by the peak height H.
- the half-value breadth ( ⁇ ) or peak height (H) of the X-ray diffraction intensity peak from other ⁇ 220 ⁇ plane is largest.
- the peak height which divides the half-value breadth is also large and this is disadvantageous in that the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak by the peak height becomes too small and many errors occur in the value itself, giving rise to poor reproducibility.
- the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane ensuring that the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak by the peak height is large (the peak height is not large and the half-value breadth is fairly large), is employed.
- the issue is absolutely the introduced state of dislocation intensity into the sheet and it is not intended to control the accumulation ratio in texture, the grain size on sheet surface or the rolled texture by the above-described X-ray diffraction intensity peak from a specific crystal plane in the sheet surface.
- the introduced state of dislocation intensity into the sheet cannot be specified or controlled by this X-ray diffraction intensity peak from a specific crystal plane in the sheet surface or the control of the accumulation ratio in texture, the grain size on sheet surface or the rolled texture.
- the strain amount introduced in the final cold rolling is increased. That is, in the final cold rolling, a technique such as use of a small-size roll having a roll diameter of less than 80 mm ⁇ or setting of the rolling reduction (cold rolling ratio) per pass to 20% or more is selected and used, or these techniques are used in combination.
- the press punchability is exactly evaluated by the "burr height" generated in a press punching test of punching a circular round hole in a copper alloy sheet according to Japan Copper and Brass Association Technical Standards JCBA T310 "Shear Test Method of Copper and Copper Alloy Thin Sheet Materials".
- the burr height is 5 ⁇ m or less, the press punchability of the Cu-Ni-Sn-P-based copper alloy sheet can be rated as good.
- test conditions enabling assurance of the reproducibility in the above-described press punching test are specifically specified. That is, in the press punching test, a punching press shown in Fig. 4(a) is used, and a copper alloy sheet (test specimen, material to be worked) held on the top of a die having a circular round hole, which is supported by a die holder, is punched from the upper side to the down side by a 10 mm ⁇ punch. The clearance with the punch is set to 3%, and the copper alloy sheet is fixed to the die top from the upper part by a platelike stopper. A lubricating oil, UNIPRESS PA5, produced by Nisseki Mitsubishi is used. The construction material of the punch and die is SKS-3, the die cutter length is 5 mm, and the punching die taper is 0°.
- Fig. 4(b) shows the side cross-section of the punched hole generated in the copper alloy sheet by the punching above.
- the side cross-section of the punched hole is observed through a scanning microscope, and the "burr height" (height of burr or flash: ⁇ m) projecting downward in the peripheral part at the bottom of the punched hole is measured.
- the "burr height" per one punched hole values at 4 points created by 90° dividing the circumference of the circular punched hole are averaged and furthermore, by punching 6 sheets (6 pieces) for each copper alloy sheet, an average of these sheets is taken as the "burr height" ( ⁇ m).
- t is the thickness of the copper alloy sheet
- a is the shear plane of the punched hole
- b is a fracture plane of punched hole
- c is a shear droop generated in the peripheral part at the top of the punched hole.
- the component composition of the copper alloy according to the embodiment of the present invention is described below.
- the component composition of the copper alloy is, as described above, a Cu-Ni-Sn-P-based alloy allowing for ingot making in a shaft furnace and because of its high productivity, enabling a great cost down.
- the copper alloy fundamentally comprises 0.1 to 3.0% of Ni, 0.01 to 3.0% of Sn and 0.01 to 0.3% of P, with the balance being copper and inevitable impurities.
- the % indicative of the content of each element means mass% including the indication in the claims.
- the alloy elements of the copper alloy according to the embodiment of the present invention are described below by referring to the reasons of incorporation (addition) or restraint.
- Ni is an element necessary for enhancing the strength or stress relaxation resistance characteristic by being present as a solid solution in the copper alloy matrix or forming a fine precipitate or compound with other alloy elements such as P. If the Ni content is less than 0.1%, even by an optimal production method, the absolute amount of a fine Ni compound of 0.1 ⁇ m or less or of Ni contained as a solid solution becomes insufficient. Accordingly, a content of 0.1% or more is necessary for effectively bringing out those effects of Ni.
- Ni is excessively contained to exceed 3.0%, a compound such as oxide, crystallized product or precipitate of Ni is coarsened or a coarse Ni compound increases, as a result, the amount of a fine Ni compound or the amount of Ni contained as a solid solution rather decreases.
- the coarsened Ni compound becomes a starting point of fracture and leads to reduction in the strength or bendability. Accordingly, the Ni content is specified to be 0.1 to 3.0%, preferably 0.3 to 2.0%.
- Sn is contained as a solid solution in the copper alloy matrix and thereby enhances the strength. Also, Sn contained as a solid solution suppresses the softening due to recrystallization during annealing. If the Sn content is less than 0.01%, the amount of Sn is too small and the strength cannot be enhanced, whereas if the Sn content exceeds 3.0%, not only the electrical conductivity is significantly decreased but also Sn contained as a solid solution is segregated in the grain boundary to reduce the strength or bendability. Accordingly, the Sn content is specified to be 0.01 to 3.0%, preferably 0.1 to 2.0%.
- P is an element necessary for enhancing the strength or stress relaxation resistance characteristic by forming a fine precipitate with Ni. Also, P acts as a deoxidizing agent. A content of less than 0.01% causes shortage in the P-based fine precipitate particle and therefore, a content of 0.01% or more is necessary. However, if this element is excessively contained to exceed 0.3%, an Ni-P intermetallic compound precipitated particle is coarsened, which leads to reduction not only in the strength or stress relaxation resistance characteristic but also in the hot workability. Accordingly, the P content is specified to be 0.01 to 0.3%, preferably 0.02 to 0.2%.
- Fe, Zn, Mn, Si and Mg are impurities that readily intermix from a molten raw material such as scrap. These elements each produces an effect when contained but generally decreases the electrical conductivity. Also, if the content is increased, ingot making in a shaft furnace becomes difficult. Accordingly, in the case of obtaining a high electrical conductivity, the contents are specified to be 0.3% or less of Fe, 0.05% or less of Zn, 0.1% or less of Mn, 0.1% or less of Si and 0.3% or less of Mg. In other words, the contents lower than these upper limits are allowable in the embodiment of the present invention.
- Fe elevates the recrystallization temperature of the copper alloy, similarly to Sn. However, if its content exceeds 0.5%, the electrical conductivity decreases. The content is 0.3% or less.
- Zn prevents separation of tin plating.
- its content exceeds 1%, the electrical conductivity decreases and a high electrical conductivity cannot be obtained.
- the content is 0.05% or less.
- the temperature region from about 150 to 180°C where the alloy sheet is used as an automotive terminal, the effect of preventing separation of tin plating can be obtained even with a content of 0.05% or less.
- Mn and Si have an effect as a deoxidizing agent. However, if the content thereof exceeds 0.1%, the electrical conductivity decreases and a high electrical conductivity cannot be obtained. In the case of ingot making in a shaft furnace, the contents are preferably 0.001% or less of Mn and 0.002% or less of Si.
- Mg has an activity of enhancing the stress relaxation resistance characteristic. However, if its content exceeds 0.3%, the electrical conductivity decreases and a high electrical conductivity cannot be obtained. In the case of ingot making in a shaft furnace, the content is preferably 0.001% or less.
- the copper alloy according to the embodiment of the present invention is allowed to further contain at least one member selected from the group consisting of Ca, Zr, Ag, Cr, Cd, Be, Ti, Co, Au and Pt in an amount of 1.0% or less in terms of a total amount of these elements.
- These elements have an activity of preventing coarsening of the grain but, if the amount of these elements exceeds 1.0% in total, the electrical conductivity decreases and a high electrical conductivity cannot be obtained. Also, ingot making in a shaft furnace becomes difficult.
- Hf, Th, Li, Na, K, Sr, Pd, W, S, C, Nb, Al, V, Y, Mo, Pb, In, Ga, Ge, As, Sb, Bi, Te, B and Misch metal are also impurities, and the amount of these elements is limited to 0.1% or less in total.
- the production method of the copper alloy sheet according to the embodiment of the present invention is described below.
- the production method itself may be an ordinary method except for the conditions in the finish annealing step. That is, a molten copper alloy after adjusting the component composition is subjected to casting, ingot scalping, soaking and hot rolling and then repeatedly to cold rolling and annealing, whereby a final (product) sheet is obtained.
- preferred production conditions are present for allowing the copper alloy sheet according to the embodiment of the present invention to obtain necessary properties such as strength, stress relaxation resistance characteristic and press punchability, and these are described below.
- the time required is preferably as short as possible, such that the time required from the completion of addition of alloy elements to the initiation of casting in the copper alloy melting furnace is within 1,200 seconds and further, the time required from the extraction of ingot out of the ingot heating furnace to the completion of hot rolling is within 1,200 seconds.
- Hot rolling may be performed in an ordinary manner.
- the inlet-side temperature of hot rolling is approximately from 600 to 1,000°C, and the finishing temperature is approximately from 600 to 850°C. After the hot rolling, water cooling or standing to cool is performed.
- cold rolling and annealing are repeatedly performed to obtain a copper alloy sheet having a product sheet thickness.
- the annealing and cold rolling may be repeated according to the final (product) sheet thickness.
- the working ratio is selected so that a working ratio of approximately from 30 to 80% can be obtained in the final finish rolling.
- intermediate recrystallization annealing may be appropriately interposed.
- the strain amount introduced in the final cold rolling is increased. That is, after setting the roll length (roll width) in the final cold rolling to 500 mm or more, a technique such as use of a small-size roll having a roll diameter of less than 80 mm ⁇ or setting of the minimum rolling reduction (cold rolling ratio, working ratio) per pass to 20% or more is selected and used, or these techniques are used in combination.
- the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface by the peak height becomes less than 1.0 ⁇ 10 -4 , making little difference from the conventional copper alloy sheet with a small dislocation density, and the stress relaxation resistance characteristic and press punchability are decreased or not enhanced.
- the rolling is preferably performed usually in 3 or 4 passes while avoiding an excessively small or large number of passes.
- the rolling reduction per pass need not exceed 50% and each rolling reduction per pass is determined by taking into consideration the original sheet thickness, final sheet thickness after cold rolling, number of passes, minimum rolling reduction per pass, and maximum rolling reduction.
- the finish annealing is preferably performed at a maximum peak temperature of 500 to 800°C in terms of the substantial temperature of the sheet, and the holding time in this temperature range is preferably from 10 to 60 seconds.
- the strain relief annealing or stabilizing annealing after the final finish cold rolling is preferably performed under the conditions of a substantial temperature of 250 to 450°C ⁇ 20 to 40 seconds. By this annealing, the strain introduced in the final finish rolling can be removed. At the same time, softening of the material does not occur and reduction in the strength can be suppressed.
- Copper alloy thin sheets varied in the half-value breadth (dislocation density) of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface were produced by changing the roll diameter and minimum rolling reduction per pass in the final cold rolling. These copper alloy thin sheets each was evaluated for various properties such as electrical conductivity, tensile strength, 0.2%-proof stress, shear plane ratio and stress relaxation resistance characteristic.
- a copper alloy having a chemical component composition shown in Table 1 (the balance of the composition excluding the element amounts shown is Cu) was melted in a coreless furnace and then subjected to ingot making by a semicontinuous casting method (cold solidification rate of casting: 2°C/sec) to obtain an ingot of 70 mm (thickness) ⁇ 200 mm (width) ⁇ 500 mm (length).
- the obtained ingots were rolled in common under the following conditions to obtain a copper alloy thin sheet.
- each ingot was scalped and heated, the ingot was heated at 960°C in a heating furnace and immediately hot-rolled at a hot rolling finishing temperature of 750°C into a 16 mm-thick sheet, and the sheet was quenched in water from a temperature of 650°C or more.
- the time required from the completion of addition of alloy elements to the initiation of casting in the melting furnace was set to 1,200 seconds or less commonly among respective Examples, and the time required from the extraction out of the heating furnace to the completion of hot rolling was set to 1,200 seconds or less commonly among respective Examples.
- the sheet was subjected to cold rolling, continuous finish annealing, cold rolling and strain relief annealing in this order to produce a copper alloy thin sheet. That is, the sheet after primary cold rolling (rough cold rolling, intermediate cold rolling) was scalped. Finish annealing of the sheet was performed in an annealing furnace at the maximum peak temperature of 600°C in terms of the substantial temperature of the sheet by holding the sheet at this temperature for 60 seconds.
- the balance of the composition excluding the element amounts shown is Cu, and the content of elements of Group A, that is, Ca, Zr, Ag, Cr, Cd, Be, Ti, Co, Au and Pt, as other impurity elements was 1.0 mass% or less in total of these elements.
- the content of elements of Group B was 0.1 mass% or less in total of these elements.
- An X-ray diffraction pattern of the copper alloy sheet sample was obtained by a normal X-ray diffraction method under the conditions of a tube voltage of 40 kV, a tube current of 200 mA, a scan rate of 2°/min, a sampling width of 0.02° and a measurement range (2 ⁇ ) of 30 to 115° by using an X-ray diffraction analyzer (Model: RINT 1500) manufactured by Rigaku Corporation and using Co as the target. From this pattern, the half-value breadth of the X-ray diffraction intensity-peak from ⁇ 200 ⁇ plane in the sheet surface was determined by the method described above. The measurement was performed at two portions and an average of the values obtained was used as the half-value breadth.
- test specimen was sampled from the copper alloy thin sheet and machined to produce a JIS No. 5 tensile test specimen such that the longitudinal direction of the test specimen runs in the direction orthogonal to the rolling direction of the sheet material.
- the proof stress is tensile strength corresponding to a permanent elongation of 0.2%.
- a sample was extracted from the copper alloy thin sheet and measured for the electrical conductivity.
- the sheet was worked into a strip-like test specimen of 10 mm (width) ⁇ 300 mm (length) by milling and measured for the electrical resistance by a double bridge-type resistance measuring apparatus according to the measuring method of electrical conductivity of nonferrous metal materials specified in JIS-H0505, and the electrical conductivity was calculated according to the average cross-sectional area method.
- the burr height of the copper alloy sheet sample was measured under the above-described test conditions.
- the sample was rated A when the burr height was 5 ⁇ m or less, rated B when the burr height was from 5 to 10 ⁇ m, and rated C when the burr height exceeded 10 ⁇ m.
- the copper alloy thin sheet was evaluated for the stress relaxation resistance characteristic in the orthogonal direction involving severer stress relaxation than in the parallel direction, with respect to the rolling direction by measuring the stress relaxation ratio in this direction.
- the stress relaxation ratio measuring test a sample where the stress relaxation ratio in the direction orthogonal to the rolling direction is less than 10% is judged as passed in terms of the stress relaxation resistance characteristic.
- a test specimen was sampled from the copper alloy thin sheet and measured using the cantilever system shown in Fig. 1 .
- L was determined such that a surface stress corresponding to 80% of the proof stress of the material was loaded on the material.
- the specimen was taken out, and the permanent distortion ⁇ after removing the deflection d was determined.
- the copper alloy sheets are produced within preferred conditions of the production method such as roll diameter and minimum rolling reduction per pass in final cold rolling. Accordingly, in Inventive Examples of Table 2, the copper alloy sheet has a dislocation density such that the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface by the peak height is 1.0 ⁇ 10 -4 or more.
- the copper alloy sheets of Inventive Examples 64 to 72 have, as terminal/connector properties, an electrical conductivity of 30% IACS or more and a stress relaxation ratio of less than 10% in the orthogonal direction involving severer stress relaxation, with respect to the rolling direction and further have, as mechanical properties, a 0.2%-proof stress of 500 MPa or more and excellent press punchability. That is, the copper alloy sheets of Inventive Examples are assured of high electrical conductivity and strength and excellent particularly in the press punchability and stress relaxation resistance characteristic, revealing that the copper alloy sheet satisfies all of these properties at the same time.
- Inventive Example 67 of Table 2 (alloy No. 51 of Table 1), the Ni content is the lower limit of 0.1%; in Inventive Example 68 (alloy No. 52 of Table 1), the Ni content is the upper limit of 3.0%; in Inventive Example 69 (alloy No. 53 of Table 1), the Sn content is the lower limit of 0.01%; in Inventive Example 70 (alloy No. 54 of Table 1), the Sn content is the upper limit of 3.0%; in Inventive Example 71 (alloy No. 55 of Table 1), the P content is the lower limit of 0.01%; and in Inventive Example 72 (alloy No. 56 of Table 1), the P content is the upper limit of 0.3%.
- the copper alloy sheets are produced within preferred conditions of the production method such as roll diameter and minimum rolling reduction per pass in final cold rolling. Accordingly, in Comparative Examples 75 to 79, the copper alloy sheet has a dislocation density such that the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface by the peak height is 1.0 ⁇ 10 -4 or more. Nevertheless, in these Comparative Examples, due to use of alloy Nos. 59 to 63 of Table 1 which are a copper alloy out of the composition range of the embodiment of the present invention, any one of the electrical conductivity, strength, stress relaxation resistance characteristic and press punchability is significantly inferior to Inventive Examples.
- Comparative Example 75 of Table 2 the Ni content deviates below the lower limit (alloy No. 59 of Table 1), as a result, the strength and stress relaxation resistance characteristic are low and the press punchability is also poor due to low strength.
- Comparative Example 76 the Ni content deviates above the upper limit (alloy No. 60 of Table 1) and therefore, the balance between strength and electrical conductivity is low.
- Comparative Example 79 the P content deviates below the lower limit (alloy No. 63 of Table 1) and therefore, the strength, stress relaxation resistance characteristic and press punchability are low.
- Comparative Example 80 the P content deviates above the upper limit (alloy No. 64 of Table 1) and therefore, cracking occurred during hot rolling, failing in characterization.
- Comparative Examples 81 and 82 of Table 2 a copper alloy within the composition range of the embodiment of the present invention in Table 1 is used (alloy Nos. 49 and 50) and other production conditions are also within the preferred range, similarly to Inventive Examples. Nevertheless, only the conditions of the final cold rolling are out of the preferred range. In Comparative Example 81, the minimum rolling reduction (%) per pass of the final cold rolling is too small, and in Comparative Example 82, the roll diameter (mm) of the final cold rolling is too large and the minimum rolling reduction (%) per pass is too small.
- Comparative Examples 81 and 82 the value obtained by dividing the half-value breadth of the X-ray diffraction intensity peak from ⁇ 200 ⁇ plane in the sheet surface by the peak height is less than 1.0 ⁇ 10 -4 and the dislocation density is too small.
- the press punchability is significantly poor as compared with Inventive Examples.
- the strength and stress relaxation resistance characteristic are also lower than in Inventive Examples.
- Element Group A the total content of Ca, Zr, Ag, Cr, Cd, Be, Ti, Co, Au and Pt.
- Other Element Group B the total content of Hf, Th, Li, Na, K, Sr, Pd, W, S, C, Nb, Al, V, Y, Mo, Pb, In, Ga, Ge, As, Sb, Bi, Te, B and Misch metal. Table 2 Class No. Alloy No.
- a Cu-Ni-Sn-P-based alloy sheet satisfying the press punchability and being excellent also in other properties required for a terminal or a connector, such as strength and stress relaxation resistance characteristic, can be provided.
- connection component such as automotive terminal or connector.
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Claims (1)
- Kaltgewalztes Kupferlegierungsblech, bestehend aus, in Form von Masse-%, 0,1 bis 3,0% von Ni, 0,01 bis 3,0% von Sn und 0,01 bis 0,3% von P, und gegebenenfalls aus mindestens einem Element, ausgewählt aus der Gruppe, bestehend aus, in Form von Masse-%, 0,3% oder weniger von Fe, 0,05% oder weniger von Zn, 0,1% oder weniger von Mn, 0,1% oder weniger von Si und 0,3% oder weniger von Mg, gegebenenfalls aus mindestens einem Element, ausgewählt aus der Gruppe, bestehend aus Ca, Zr, Ag, Cr, Cd, Be, Ti, Co, Au und Pt, in einer Gesamtmenge von 1,0 Masse-% oder weniger, und gegebenenfalls aus mindestens einem Element, ausgewählt aus der Gruppe, bestehend aus Hf, Th, Li, Na, K, Sr, Pd, W, S, C, Nb, Al, V, Y, Mo, Pb, In, Ga, Ge, As, Sb, Bi, Te, B und Mischmetall, in einer Gesamtmenge von 0,1 Masse-% oder weniger, wobei der Rest Kupfer ist, wobei ein Wert, erhalten durch Dividieren einer Halbwertsbreite einer Röntgenbeugungsintensitätspeaks aus einer {200}-Ebene in der Blechoberfläche durch eine Höhe des Peaks, 1,0 x 10-4 oder mehr beträgt, und wobei das Kupferlegierungsblech, als Anschluss-/Verbindungsteileigenschaften, eine elektrische Leitfähigkeit von 30% IACS oder mehr aufweist.
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JP2007205630A JP4324627B2 (ja) | 2007-08-07 | 2007-08-07 | 強度−延性バランスに優れた銅合金板 |
JP2007232641A JP4210703B1 (ja) | 2007-09-07 | 2007-09-07 | 耐応力緩和特性と曲げ加工性とに優れた銅合金板 |
JP2007252036A JP4210705B1 (ja) | 2007-09-27 | 2007-09-27 | 耐応力緩和特性とプレス打ち抜き性とに優れた銅合金板 |
JP2007252037A JP4210706B1 (ja) | 2007-09-27 | 2007-09-27 | 耐応力緩和特性に優れた銅合金板 |
EP08791572.4A EP2184371B1 (de) | 2007-08-07 | 2008-07-24 | Kupferlegierungsblech |
PCT/JP2008/063320 WO2009019990A1 (ja) | 2007-08-07 | 2008-07-24 | 銅合金板 |
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EP13005147.7A Active EP2695956B1 (de) | 2007-08-07 | 2008-07-24 | Kupferlegierungsblech |
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Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102197151B (zh) * | 2008-10-22 | 2013-09-11 | 古河电气工业株式会社 | 铜合金材料、电气电子部件以及铜合金材料的制造方法 |
CN101440445B (zh) | 2008-12-23 | 2010-07-07 | 路达(厦门)工业有限公司 | 无铅易切削铝黄铜合金及其制造方法 |
JP4831258B2 (ja) * | 2010-03-18 | 2011-12-07 | 三菱マテリアル株式会社 | スパッタリングターゲット及びその製造方法 |
JP5714863B2 (ja) * | 2010-10-14 | 2015-05-07 | 矢崎総業株式会社 | 雌端子および雌端子の製造方法 |
KR20140025607A (ko) * | 2011-08-04 | 2014-03-04 | 가부시키가이샤 고베 세이코쇼 | 구리 합금 |
JP5117604B1 (ja) * | 2011-08-29 | 2013-01-16 | Jx日鉱日石金属株式会社 | Cu−Ni−Si系合金及びその製造方法 |
JP5126436B1 (ja) * | 2012-02-17 | 2013-01-23 | 日立電線株式会社 | 圧延銅箔 |
US9002499B2 (en) * | 2012-03-20 | 2015-04-07 | GM Global Technology Operations LLC | Methods for determining a recovery state of a metal alloy |
JP5470483B1 (ja) * | 2012-10-22 | 2014-04-16 | Jx日鉱日石金属株式会社 | 導電性及び応力緩和特性に優れる銅合金板 |
JP5417523B1 (ja) * | 2012-12-28 | 2014-02-19 | 三菱マテリアル株式会社 | 電子・電気機器用銅合金、電子・電気機器用銅合金薄板、電子・電気機器用導電部品及び端子 |
KR101274063B1 (ko) * | 2013-01-22 | 2013-06-12 | 한국기계연구원 | 배향된 석출물을 가지는 금속복합재료 및 이의 제조방법 |
JP5417539B1 (ja) * | 2013-01-28 | 2014-02-19 | 三菱マテリアル株式会社 | 電子・電気機器用銅合金、電子・電気機器用銅合金薄板、電子・電気機器用導電部品及び端子 |
JP5501495B1 (ja) * | 2013-03-18 | 2014-05-21 | 三菱マテリアル株式会社 | 電子・電気機器用銅合金、電子・電気機器用銅合金薄板、電子・電気機器用導電部品及び端子 |
JP5604549B2 (ja) * | 2013-03-18 | 2014-10-08 | 三菱マテリアル株式会社 | 電子・電気機器用銅合金、電子・電気機器用銅合金薄板、電子・電気機器用導電部品及び端子 |
CN103421983B (zh) * | 2013-08-23 | 2015-08-19 | 苏州长盛机电有限公司 | 一种铜镍锌合金的制备方法 |
CN103526070A (zh) * | 2013-09-29 | 2014-01-22 | 苏州市凯业金属制品有限公司 | 一种硅青铜合金金属管 |
JP6050738B2 (ja) * | 2013-11-25 | 2016-12-21 | Jx金属株式会社 | 導電性、成形加工性および応力緩和特性に優れる銅合金板 |
CN104046813B (zh) * | 2014-06-05 | 2016-06-29 | 锐展(铜陵)科技有限公司 | 一种汽车电线电缆用高强高导铜合金线的制备方法 |
WO2016071498A1 (de) * | 2014-11-06 | 2016-05-12 | Hirschmann Car Communication Gmbh | Kontaktierungspin aus kupferdraht |
WO2016171054A1 (ja) * | 2015-04-24 | 2016-10-27 | 古河電気工業株式会社 | 銅合金板材およびその製造方法 |
CN104928528A (zh) * | 2015-07-06 | 2015-09-23 | 苏州科茂电子材料科技有限公司 | 一种导电铜合金材料及其制备方法 |
CN105063418B (zh) * | 2015-07-24 | 2017-04-26 | 宁波金田铜业(集团)股份有限公司 | 一种低合金化铜带的制备方法 |
CN105400989A (zh) * | 2015-11-13 | 2016-03-16 | 太仓荣中机电科技有限公司 | 一种含稀土元素的电子合金材料 |
KR101627696B1 (ko) | 2015-12-28 | 2016-06-07 | 주식회사 풍산 | 자동차 및 전기전자 부품용 동합금재 및 그의 제조 방법 |
CN107046763B (zh) * | 2016-02-05 | 2019-12-24 | Jx金属株式会社 | 柔性印刷基板用铜箔、使用其的覆铜层叠体 |
CN106987739B (zh) * | 2017-04-05 | 2018-10-26 | 浙江大学 | 用于高铁接触线的铜合金及其制备方法 |
CN107723499A (zh) * | 2017-09-20 | 2018-02-23 | 宁波兴敖达金属新材料有限公司 | 无铅易切削高强度高塑性高导电率的碲银铬青铜材料 |
JP6648088B2 (ja) * | 2017-10-19 | 2020-02-14 | Jx金属株式会社 | 二次電池負極集電体用圧延銅箔、それを用いた二次電池負極及び二次電池並びに二次電池負極集電体用圧延銅箔の製造方法 |
EP3531510B1 (de) * | 2018-02-23 | 2023-01-04 | Borgwarner Inc. | Kontaktanordnung für hochstromanwendungen |
CN109022900B (zh) * | 2018-08-17 | 2020-05-08 | 宁波博威合金材料股份有限公司 | 一种综合性能优异的铜合金及其应用 |
CN112889175A (zh) * | 2018-11-06 | 2021-06-01 | 利萨·德雷克塞迈尔有限责任公司 | 用于机动车辆电池的各圆形电池单元的导电连接的电池单元连接件以及用于制造机动车辆电池的方法 |
CN110066942B (zh) * | 2019-04-28 | 2020-12-29 | 中南大学 | 一种超高强高韧高导电铜镍锡合金及其制备方法 |
CN110306077B (zh) * | 2019-07-24 | 2021-12-03 | 宁波兴业盛泰集团有限公司 | 一种电连接器用耐蚀铜合金及其制备方法 |
CN110885937B (zh) * | 2019-12-19 | 2021-04-13 | 福州大学 | 一种Cu-Ti-Ge-Ni-X铜合金材料及其制备方法 |
CN114318055B (zh) * | 2022-01-07 | 2022-12-09 | 江西省科学院应用物理研究所 | 一种高强高导高韧铜合金及其制备方法 |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5816044A (ja) * | 1981-07-23 | 1983-01-29 | Mitsubishi Electric Corp | 銅基合金 |
JPS6039142A (ja) * | 1983-08-11 | 1985-02-28 | Mitsubishi Electric Corp | 銅基合金 |
JPS60245753A (ja) * | 1984-05-22 | 1985-12-05 | Nippon Mining Co Ltd | 高力高導電銅合金 |
JPS6299430A (ja) * | 1985-10-26 | 1987-05-08 | Dowa Mining Co Ltd | 端子・コネクタ−用銅基合金およびその製造法 |
JPS62227052A (ja) * | 1986-03-28 | 1987-10-06 | Dowa Mining Co Ltd | 端子・コネクター用銅基合金の製造法 |
JP2844120B2 (ja) * | 1990-10-17 | 1999-01-06 | 同和鉱業株式会社 | コネクタ用銅基合金の製造法 |
US5387293A (en) * | 1991-01-17 | 1995-02-07 | Dowa Mining Co., Ltd. | Copper base alloys and terminals using the same |
JPH10226835A (ja) * | 1997-02-18 | 1998-08-25 | Dowa Mining Co Ltd | 端子用銅基合金とそれを用いた端子 |
JP3510469B2 (ja) * | 1998-01-30 | 2004-03-29 | 古河電気工業株式会社 | 導電性ばね用銅合金及びその製造方法 |
JP3748709B2 (ja) | 1998-04-13 | 2006-02-22 | 株式会社神戸製鋼所 | 耐応力緩和特性に優れた銅合金板及びその製造方法 |
JP3344700B2 (ja) * | 1998-06-01 | 2002-11-11 | 株式会社神戸製鋼所 | プレス打ち抜き加工時の熱処理性に優れる高強度、高導電性リードフレーム用銅合金板 |
JP2000129377A (ja) * | 1998-10-28 | 2000-05-09 | Sumitomo Metal Mining Co Ltd | 端子用銅基合金 |
JP2000256814A (ja) * | 1999-03-03 | 2000-09-19 | Sumitomo Metal Mining Co Ltd | 端子用銅基合金条の製造方法 |
JP4056175B2 (ja) | 1999-05-13 | 2008-03-05 | 株式会社神戸製鋼所 | プレス打抜き性が優れたリードフレーム、端子、コネクタ、スイッチ又はリレー用銅合金板 |
JP2000328157A (ja) | 1999-05-13 | 2000-11-28 | Kobe Steel Ltd | 曲げ加工性が優れた銅合金板 |
JP4393663B2 (ja) * | 2000-03-17 | 2010-01-06 | 住友金属鉱山株式会社 | 端子用銅基合金条およびその製造方法 |
JP4396874B2 (ja) * | 2000-03-17 | 2010-01-13 | 住友金属鉱山株式会社 | 端子用銅基合金条の製造方法 |
JP4729680B2 (ja) * | 2000-12-18 | 2011-07-20 | Dowaメタルテック株式会社 | プレス打ち抜き性に優れた銅基合金 |
JP3744810B2 (ja) | 2001-03-30 | 2006-02-15 | 株式会社神戸製鋼所 | 端子・コネクタ用銅合金及びその製造方法 |
JP3798260B2 (ja) | 2001-05-17 | 2006-07-19 | 株式会社神戸製鋼所 | 電気電子部品用銅合金及び電気電子部品 |
JP4087307B2 (ja) | 2003-07-09 | 2008-05-21 | 日鉱金属株式会社 | 延性に優れた高力高導電性銅合金 |
JP4041452B2 (ja) * | 2003-11-05 | 2008-01-30 | 株式会社神戸製鋼所 | 耐熱性に優れた銅合金の製法 |
JP4660735B2 (ja) * | 2004-07-01 | 2011-03-30 | Dowaメタルテック株式会社 | 銅基合金板材の製造方法 |
JP3962751B2 (ja) * | 2004-08-17 | 2007-08-22 | 株式会社神戸製鋼所 | 曲げ加工性を備えた電気電子部品用銅合金板 |
JP4524471B2 (ja) * | 2004-08-30 | 2010-08-18 | Dowaメタルテック株式会社 | 銅合金箔およびその製造法 |
JP4350049B2 (ja) | 2005-02-07 | 2009-10-21 | 株式会社神戸製鋼所 | 耐応力緩和特性に優れた銅合金板の製造方法 |
JP3871064B2 (ja) * | 2005-06-08 | 2007-01-24 | 株式会社神戸製鋼所 | 電気接続部品用銅合金板 |
CN101693960B (zh) * | 2005-06-08 | 2011-09-07 | 株式会社神户制钢所 | 铜合金、铜合金板及其制造方法 |
JP4680765B2 (ja) * | 2005-12-22 | 2011-05-11 | 株式会社神戸製鋼所 | 耐応力緩和特性に優れた銅合金 |
JP4117327B2 (ja) * | 2006-07-21 | 2008-07-16 | 株式会社神戸製鋼所 | プレス打ち抜き性に優れた電気電子部品用銅合金板 |
-
2008
- 2008-07-24 KR KR1020107002597A patent/KR101227315B1/ko active IP Right Grant
- 2008-07-24 EP EP13005148.5A patent/EP2695957B1/de active Active
- 2008-07-24 CN CN200880024723A patent/CN101743333A/zh active Pending
- 2008-07-24 EP EP08791572.4A patent/EP2184371B1/de active Active
- 2008-07-24 WO PCT/JP2008/063320 patent/WO2009019990A1/ja active Application Filing
- 2008-07-24 EP EP13005147.7A patent/EP2695956B1/de active Active
- 2008-07-24 US US12/672,092 patent/US20110223056A1/en not_active Abandoned
- 2008-07-24 EP EP13005149.3A patent/EP2695958B1/de active Active
Non-Patent Citations (1)
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Also Published As
Publication number | Publication date |
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EP2695957A3 (de) | 2014-07-02 |
EP2184371A4 (de) | 2013-05-01 |
EP2184371A1 (de) | 2010-05-12 |
EP2695958B1 (de) | 2018-12-26 |
EP2695956A2 (de) | 2014-02-12 |
EP2695957A2 (de) | 2014-02-12 |
CN101743333A (zh) | 2010-06-16 |
EP2184371B1 (de) | 2016-11-30 |
KR20100031138A (ko) | 2010-03-19 |
KR101227315B1 (ko) | 2013-01-28 |
EP2695956B1 (de) | 2018-12-19 |
EP2695958A3 (de) | 2014-07-02 |
EP2695958A2 (de) | 2014-02-12 |
EP2695956A3 (de) | 2014-06-18 |
US20110223056A1 (en) | 2011-09-15 |
WO2009019990A1 (ja) | 2009-02-12 |
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