EP1473374B1 - Alliage de cuivre - Google Patents
Alliage de cuivre Download PDFInfo
- Publication number
- EP1473374B1 EP1473374B1 EP04009838A EP04009838A EP1473374B1 EP 1473374 B1 EP1473374 B1 EP 1473374B1 EP 04009838 A EP04009838 A EP 04009838A EP 04009838 A EP04009838 A EP 04009838A EP 1473374 B1 EP1473374 B1 EP 1473374B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alloy
- copper alloy
- content
- thermal expansion
- expansion coefficient
- 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 - Lifetime
Links
- 229910000881 Cu alloy Inorganic materials 0.000 title claims abstract description 73
- 239000010949 copper Substances 0.000 claims abstract description 66
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 31
- 239000000956 alloy Substances 0.000 claims abstract description 27
- 229910052742 iron Inorganic materials 0.000 claims abstract description 27
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 26
- 229910052802 copper Inorganic materials 0.000 claims abstract description 26
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 26
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 26
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 26
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 21
- 238000005266 casting Methods 0.000 claims abstract description 15
- 229910000765 intermetallic Inorganic materials 0.000 claims description 28
- 239000000843 powder Substances 0.000 claims description 24
- 238000005245 sintering Methods 0.000 claims description 16
- 239000012535 impurity Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 abstract description 24
- 229910000521 B alloy Inorganic materials 0.000 abstract description 10
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 9
- 229910052751 metal Inorganic materials 0.000 abstract description 6
- 239000002184 metal Substances 0.000 abstract description 6
- 238000010438 heat treatment Methods 0.000 abstract description 5
- 238000005098 hot rolling Methods 0.000 abstract description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 3
- 239000001301 oxygen Substances 0.000 abstract description 3
- 229910052760 oxygen Inorganic materials 0.000 abstract description 3
- 229910017818 Cu—Mg Inorganic materials 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 28
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 23
- 229910001080 W alloy Inorganic materials 0.000 description 10
- 230000003287 optical effect Effects 0.000 description 9
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 229910001182 Mo alloy Inorganic materials 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 229910052750 molybdenum Inorganic materials 0.000 description 6
- 229910020674 Co—B Inorganic materials 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 238000004891 communication Methods 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 229910052721 tungsten Inorganic materials 0.000 description 5
- 229910008423 Si—B Inorganic materials 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 229910017076 Fe Zr Inorganic materials 0.000 description 3
- 229910001030 Iron–nickel alloy Inorganic materials 0.000 description 3
- 229910017709 Ni Co Inorganic materials 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 230000008595 infiltration Effects 0.000 description 3
- 238000001764 infiltration Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910002056 binary alloy Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910000906 Bronze Inorganic materials 0.000 description 1
- 229910020073 MgB2 Inorganic materials 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000010587 phase diagram Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
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
-
- 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
- C22C9/01—Alloys based on copper with aluminium 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
- C22C9/05—Alloys based on copper with manganese 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
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/10—Alloys based on copper with silicon as the next major constituent
Definitions
- the present invention relates to lead frames, optical communication connector cases, optical amplifier cases, and heat sinks for semiconductor devices.
- the material conventionally used for lead frames for integrated circuit devices and so forth is, for example, an Fe-Ni alloy or a Cu alloy which has comparable of thermal expansion coefficients as that of Si as a material for device.
- Cu, Al, Au, Mo, and their alloys or Cu-W alloys and Cu-Mo alloys which are excellent in thermal conductivity are used as materials for a heat sink which dissipates the heat generated from a CPU (Central Processing Unit), and which are provided inside or outside of the package of a personal computer (refer to Japanese Unexamined Patent Application, First Publication No. Hei 10-8166 , pages 2 to 3).
- a material which has almost the same thermal expansion coefficient as a material for device such as Si and which is capable of dissipating the generated heat is required as a material for a lead frame.
- Cu or conventional Cu alloy has high thermal conductivity, it is distorted by heat due to a higher heat expansion coefficient than a material for device.
- Cu-W alloys, Cu-Mo alloys, and so forth have high thermal conductivity and lower thermal expansion coefficients than conventional Al, Cu, and Cu alloys, and it is thereby possible to approximate the thermal expansion coefficient of these alloys to that of ceramics; however, these alloys are expensive. If elemental Mo is used, it is expensive and is difficult to machine to form a heat sink due to the high strength.
- Cu-W alloys and Cu-Mo alloys are generally manufactured by an infiltration method in which powders of W and Mo are sinter molded to be sponge-like, and the sponge-like W and Mo are impregnated with molten Cu, since W and Mo have high melting point, and W and Mo do not react each other.
- the impregnation is technically difficult and process yield is low, and then the manufacturing cost is increased.
- elemental Mo it is expensive and it is difficult to machine it to form a heat sink due to the high strength thereof.
- US 4818307 discloses a Cu alloy with a dispersion of hard particles of silicides further composed with borides of Fe-Ni in complex form.
- the Cu alloy is directed to a wear resistant material.
- An object of the present invention is to provide a copper alloy which has superior thermal conductivity which is comparable to that of the conventional material, a lower thermal expansion coefficient than conventional copper, and is capable of being produced at a lower cost.
- the first aspect of the present invention is a copper alloy comprising B at 0.01 to 10.0 % by weight, and at least one element selected from the group of Ni, Co, Al, Si, Fe, Zr, and Mn at 0.05 to 40.0 % by weight in total amount, the balance containing Cu and inevitable impurities, and total volume ratio of elemental B and an intermetallic compound of B with at least one element selected from the group of Cu, Ni, Co, Al, Si, Fe, Zr, and Mn at 1 to 80 % by volume based on total volume, and the content of A1 by weight is not more than 10 times the weight of B.
- a group of intermetallic compounds comprising B elemental phase, Cu-B alloy phase, Cu-X-B alloy phase, and X-B alloy phase all having low thermal expansion coefficients are formed in Cu, and this compound becomes a copper alloy having high thermal conductivity and low thermal expansion coefficient.
- X represents at least one element selected from the group of Ni, Co, Al, Si, Fe, Zr, and Mn. Since Al is included in the alloy, by controlling the content of Al to be no more than 10 times that of B, the thermal expansion coefficient is prevented from becoming high by using Al having a high thermal expansion coefficient.
- the above copper alloy comprising B at 0.1 to 9.8 % by weight, and 0.5 to 40.0 % by weight in total of at least one element selected from the group of Ni, Co, Al, Si, Fe, Zr and Mn, and the balance containing Cu and inevitable impurities, and the total volume ratio of an elemental B and an intermetallic compound of B with at least one element selected from the group of Cu, Ni, Co, Al, Si, Fe, Zr, and Mn at 3.0 to 74.5 % by volume based on total volume, is preferable.
- the above copper alloy includes Al, for example, Al-B intermetallic compound is formed.
- the above copper alloy of the present invention does not exhibit high thermal expansion coefficient since the Al-B intermetallic compound has low thermal expansion coefficient, even though the Al having a high thermal expansion coefficient is used.
- the copper alloy of the present invention is, for example, manufactured by a casting process or powder sintering method.
- a copper alloy having high thermal conductivity and low thermal expansion coefficient due to the group of intermetallic B compounds having low thermal expansion coefficient is formed in Cu.
- B forms intermetallic compounds reacting with other elements easily, and it allows production of an alloy by the casting process from molten metal or the powder sintering method, and thereby the production cost can be reduced.
- the copper alloy of the present invention will be explained in detail.
- the inventors of the present application discovered that Cu-X-B alloy are effective materials to solve the problem.
- X represents at least one element selected from the group of Ni, Co, Al, Si, Fe, Zr, and Mn.
- the copper alloy of the present invention has superior thermal conductivity and electrical conductivity comparable to that of the conventional copper alloy and has lower thermal expansion coefficient than copper.
- a copper alloy which is in the state including copper at no less than 20 % by volume has high thermal conductivity no less than 100W/m ⁇ K, and this results in superior performance comparable to that of Cu-W alloy, Mo and so forth, in applications which require dissipating heat.
- the copper alloy in the present invention may be produced by the casting process since the melting temperature decreases by the interaction between B or X and Cu, and by forming intermetallic compound of X and B, although B or X have high melting temperature. Furthermore, the copper alloy in the present invention may be produced by the powder sintering method in the case in which the component segregates inside the alloy material by using a casting process. In this powder sintering method, the copper alloy in the present invention may be produced at low sintering temperature since B or X reacts with Cu.
- the copper alloy in the present invention is produced inexpensively in comparison with Cu-W alloys and Cu-Mo alloys which are produced by an infiltration method since the copper alloy of the present invention is easier to solid-disperse in Cu with a phase comprising other elements than is the conventional copper alloy.
- B has a low thermal expansion coefficient
- B when B is added to Cu, a phase having a low thermal expansion coefficient in Cu is formed.
- B is easy to mix or chemically combine with other elements, and the phase including B is thereby easy to disperse into Cu. Accordingly, by adding B to Cu, a copper alloy having low thermal expansion coefficient and homogeneous characteristics can be obtained. If the content of B is less than 0.01 % by weight, the thermal expansion coefficient and thermal conductivity are comparable to those of Cu and no effect of further addition could be obtained. On the other hand, if the content of B is more than 10.0 % by weight, the deviation of thermal expansion coefficient in each production lot become big and difficult to handle because of the brittleness of the material. It is preferable that the content of B be from 0.1 to 8.1 % by weight and that the content of volume ratio of elemental B and Cu-B intermetallic compound be from 0.6 to 39.0 % by volume.
- total amount is from 0.05 to 40.0 % by weight
- Cu alloys according to the present invention exist in the state of intermetallic compounds of Al, Si, and Zr with Cu, which includes B. If the content of Si, or Zr is less than 0.05 % by weight, the advantage of addition could not be obtained since the thermal expansion coefficient and thermal conductivity are comparable to that of copper. On the other hand, if the content of any of these elements is more than 40.0 % by weight, cracks occur and the compact is difficult to use as a compact.
- Co and Fe are elements which do not solid disperse with Cu; however, in the copper alloy of the present invention, Co and Fe form intermetallic compounds having low thermal expansion coefficients by bonding B, and they maintain the state of intermetallic compounds.
- the intermetallic compounds comprising B and Co and/or Fe, has a lower melting point than elements in the elemental state and thereby the intermetallic compound melts at a lower temperature, the segregation while casting and fine dispersion is performed. Elemental Ni is solid dispersible with Cu; however, Ni-B alloy compounds do not significantly solid disperse with Cu and thereby Ni-B-Cu alloy behave in the same ways as the above Co and Fe-B alloy compounds. At this time, when the addition amount of Co, Fe, and Ni is less than 0.05% by weight, the thermal expansion coefficient does not decrease.
- the content of B be from 0.1 to 9.8 % by weight and that the total content of at least one element selected from the group of Ni, Co, Al, Si, Fe, Zr, and Mn be at 0.5 to 40.0 % by weight.
- the thermal expansion coefficient of the alloy decreases insufficiently in comparison with that of Cu.
- the volume content ratio of elemental B, and intermetallic compound of B with at least one element selected from Cu, Ni, Co, Al, Si, Fe, Zr, and Mn is more than 80.0 % by volume, the thermal conductivity falls below 100 W/m ⁇ K which is the value comparable to those of Cu-W alloys, Mo, and so forth.
- the total volume ratio of the intermetallic compound of Cu with elemental B, and at least one element selected from the group of Ni, Co, Al, Si, Fe, Zr, and Mn is from 3.0 to 74.5 % by volume in total volume.
- the content of Al 10 times or less of the content of B (mass ratio)
- Al as an element has as high a thermal expansion coefficient as Mg; however, the thermal expansion coefficient decreases by bonding B and by forming Al-B intermetallic compounds.
- the content of Al in copper alloy is controlled to be 10 times or less of the content of B in mass ratio.
- the ratio of Al is higher than 10 times of B in mass ratio, an Al phase having a high thermal expansion coefficient is formed, and the thermal expansion coefficient become higher than that of Cu.
- the copper alloy of the present invention is produced by the casting process or the powder sintering method.
- the casting process for example, Cu or the raw material of Cu-B and Ni-B is melted and cast by the high-frequency melting method. In these processes, the melting temperature and the controlling of atmosphere and so forth are timely adjusted depending on the material used. After soaking at 600 to 1000°C, a hot rolling, a cold strip, and other processes are performed, and the alloy is molded to a predetermined shape.
- the alloy may be produced by the powder sintering method.
- Cu or Cu-B powder, and at least one element selected from Ni, Co, Al, Si, Fe, Zr, and Mn, and powder produced from these element and B are mixed to be a objective component and a mold of predetermined shape is used and these powder are sintered at 600 to 900°C in an inert gas.
- the above powder sintering method is preferably applied when the content of B is at least 5 % by weight or the content of other added elements is at least 20% by weight.
- the copper alloy according to the present invention is processed to form lead frames, optical communication connector cases, and heat sinks for semiconductor devices and so forth. These compact using the copper alloy according to the present invention have lower thermal expansion coefficient than that of the compact using copper, and the electrical conductivity and thermal conductivity are superior to those of the conventional compact using Fe-42Ni and so forth.
- the copper alloy according to the present invention has at least 100 W/m ⁇ K (approximately 1/4 of that of Cu) of thermal conductivity at the same level of those of Cu-W alloy, Mo, and so forth which are used for the conventional optical communication connector cases, heat sinks for semiconductor devices, and so forth.
- the copper alloy of the present invention can be provided at lower cost than these alloys.
- a copper alloy according to the present invention by adding B, and at least one element selected from a group of Ni, Co, Al, Si, Fe, Zr, and Mn to Cu, B group intermetallic compound having low thermal expansion coefficient in Cu is formed, thereby the material having low thermal expansion coefficient can be produced while maintaining high thermal conductivity which is a feature of the copper alloy. Since B easily generates intermetallic compounds reacting with other elements, the copper alloy can be produced by a casting process from molten metal which is a relatively easy method.
- the copper alloy of the present invention can be produced by the powder sintering method.
- the copper alloy can be produced at lower cost than Cu-W alloys, Cu-Mo alloys, and so forth those are produced by special production methods such as the infiltration method. By selecting low-cost B compounds which are added to the alloy, the raw material cost can be reduced.
- the thermal expansion coefficient and thermal conductivity were measured for the above copper alloys of Reference Examples 1 to 3, the copper alloy of Comparative Example 1, Cu (Comparative Example 2), Mo (Comparative Example 3) and Fe-42Ni (Comparative Example 4).
- the thermal expansion coefficient was measured by a differential transformer method within the range from 20 to 150°C, and the average was taken.
- the thermal conductivity was measured in accordance with Japanese Industrial Standard JIS-A1412, at 25°C.
- the volume content was calculated from data measured from phase areas of B or phase areas including B, based on the total area, by taking some photos at 100 to 400 magnification of each sample. These results are shown in Table 1.
- copper alloys of Reference Examples 1 to 3 have a thermal expansion coefficient lower than that of Cu, and a thermal conductivity higher than 100 W/m ⁇ K.
- the copper alloy of Comparative Example 1 whose ratio of elements except Cu by volume is higher than the range according to the present invention, have a thermal conductivity lower than 100 W/m ⁇ K and sufficient heat dissipation cannot be expected.
- the copper alloy of the Comparative Example 1 is produced by the powder sintering method, the sintered body was extremely brittle and difficult to handle.
- the high frequency melting method was employed.
- the oxygen free high conductivity copper, base material of Cu-B alloy, and so forth were melted to a molten state in vacuo or in an Ar atmosphere, B and at least one element selected from Mg, Ni, Co, Al, Si, Fe, Zr, and/or Mn was added to the molten metal wherein the content of each element or the alloy ofNi-B, Fe-B, Cu-Mg, and so forth becoming the predetermined content.
- the copper alloys of Examples 7 to 36 which are produced within the range of the present invention, have lower thermal expansion coefficients than that of copper and higher thermal conductivities than 100 W/m ⁇ K.
- the copper alloy of Comparative Examples 5 and 6, which are outside of the range of the present invention shown in Table 4 have higher thermal conductivity than that of Cu shown in Table 1. This result occurred because Mg, which was solidly dispersed in Cu, makes the thermal expansion coefficient of the alloy high due to the content of Mg being 5 times or more the content of B in mass ratio.
- the alloy of Comparative Example 10 has a higher thermal expansion coefficient of that of Cu due to the content of Al being 10 times or more than the content of B in mass ratio.
- the content of B and Zr are within the range of the present invention; however, the thermal expansion coefficient of the alloy was lower than that of Cu and the thermal conductivity was under 100 W/m ⁇ K due to the volume ratio of B and the intermetallic compound including B exceeded 80 % by volume.
- the materials exhibited cracks during the casting process and a test piece for the measurement could not be obtained, even in the powder sintering process, due to the addition content of elements other than B exceeding 40 % by weight.
- the copper alloys of Comparative Examples 9 and 12 were extremely brittle due to the addition content of the elements other than B exceeding 40 % by weight, and the thermal conductivity was lower than 100 W/m ⁇ K due to the volume content of the intermetallic compound exceeding 80 % by volume. Accordingly, the invention is not to be considered as being limited by the foregoing description, and is only limited by the scope of the appended claims.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Cooling Or The Like Of Semiconductors Or Solid State Devices (AREA)
- Conductive Materials (AREA)
Claims (4)
- Alliage de cuivre comprenant :0,01 à 10,0 % en poids de B, etau moins un élément choisi dans le groupe Ni, Co, Al, Si, Fe, Zr et Mn à 0,05 à 40,0 % en poids de la quantité totale,le reste étant constitué de Cu et d'inévitables impuretés, etle rapport en volume total de l'élément B et d'un composé intermétallique de B avec au moins un élément choisi dans le groupe Cu, Ni, Co, Al, Si, Fe, Zr et Mn est compris entre 1 et 80 % en volume sur la base du volume total, etle contenu en Al en poids n'est pas supérieur à 10 fois le contenu en B en poids,la conductivité thermique de l'alliage de cuivre est au moins égale à 100 W/m·K, et le coefficient de dilatation thermique de l'alliage de cuivre est inférieur au coefficient de dilatation thermique du Cu (17,3 x 10-6/K).
- Alliage de cuivre selon la revendication 1, dans lequel
le contenu en B est compris entre 0,1 et 9,8 % en poids,
le contenu en au moins un élément choisi dans le groupe Ni, Co, Al, Si, Fe, Zr et Mn est compris entre 0,5 et 40 % en poids de la quantité totale, et le rapport en volume total de l'élément B et du composé intermétallique de B avec au moins un élément choisi dans le groupe Cu, Ni, Co, Al, Si, Fe, Zr et Mn est compris entre 3,0 et 74,5 % en volume sur la base du volume total. - Alliage de cuivre selon l'une quelconque des revendications 1 à 2, dans lequel l'alliage est fabriqué par un procédé de fonte.
- Alliage de cuivre selon l'une quelconque des revendications 1 à 2, dans lequel l'alliage est fabriqué par un procédé de frittage de poudre.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003124746A JP4360832B2 (ja) | 2003-04-30 | 2003-04-30 | 銅合金 |
JP2003124746 | 2003-04-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1473374A1 EP1473374A1 (fr) | 2004-11-03 |
EP1473374B1 true EP1473374B1 (fr) | 2010-01-27 |
Family
ID=32985579
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP04009838A Expired - Lifetime EP1473374B1 (fr) | 2003-04-30 | 2004-04-26 | Alliage de cuivre |
Country Status (5)
Country | Link |
---|---|
US (1) | US20040261913A1 (fr) |
EP (1) | EP1473374B1 (fr) |
JP (1) | JP4360832B2 (fr) |
AT (1) | ATE456681T1 (fr) |
DE (1) | DE602004025310D1 (fr) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4571471B2 (ja) * | 2004-09-30 | 2010-10-27 | Dowaホールディングス株式会社 | 銅合金およびその製造法ならびに放熱板 |
BRPI0817746B1 (pt) * | 2007-10-24 | 2019-04-24 | Heraeus Electro-Nite International N.V. | Sistema de termopar para medição de temperatura de metais fundidos |
US20130280120A1 (en) * | 2010-04-23 | 2013-10-24 | United States Department Of Energy | Hard and Super-hard Metal Alloys and Methods for Making the Same |
JP5218621B2 (ja) * | 2011-10-28 | 2013-06-26 | 日立金属株式会社 | 回路基板およびこれを用いた半導体モジュール |
WO2014069318A1 (fr) | 2012-11-01 | 2014-05-08 | 日本碍子株式会社 | Alliage de cuivre et son procédé de fabrication |
RU2566098C1 (ru) * | 2014-12-22 | 2015-10-20 | Юлия Алексеевна Щепочкина | Сплав на основе меди |
CN111534708B (zh) * | 2020-04-23 | 2021-04-30 | 西安斯瑞先进铜合金科技有限公司 | 一种采用真空感应熔炼制备CuMn12Ni合金的方法 |
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US2175223A (en) * | 1938-07-01 | 1939-10-10 | American Brass Co | Copper alloy |
GB536893A (en) * | 1939-12-01 | 1941-05-30 | American Brass Co | Improvements in or relating to processes for producing copper base boron alloys, and oxygen-free copper base boron alloys of high electrical conductivity |
US2809889A (en) * | 1955-11-16 | 1957-10-15 | Owens Illinois Glass Co | Aluminum bronze alloy containing boron and nickel |
US2854332A (en) * | 1956-10-11 | 1958-09-30 | Armour Res Found | Copper base brazing alloys containing boron and iron |
US3640779A (en) * | 1969-09-30 | 1972-02-08 | Olin Corp | High-conductivity copper alloys |
SU430176A1 (ru) * | 1972-03-10 | 1974-05-30 | Сплав на основе меди | |
SU544698A1 (ru) * | 1975-05-07 | 1977-01-30 | Государственный Научно-Исследовательский И Проектный Институт Сплавов И Обработки Цветных Металлов | Сплав на основе меди |
US4517157A (en) * | 1984-10-11 | 1985-05-14 | Gte Products Corporation | Copper based brazing alloy |
US4836982A (en) * | 1984-10-19 | 1989-06-06 | Martin Marietta Corporation | Rapid solidification of metal-second phase composites |
CH667880A5 (fr) * | 1986-07-30 | 1988-11-15 | Claude Planchamp | Absorbeur de radiations nucleaires. |
JPH08942B2 (ja) * | 1986-12-19 | 1996-01-10 | トヨタ自動車株式会社 | 分散強化Cu基合金 |
DE3725950A1 (de) * | 1987-08-05 | 1989-02-16 | Kabel Metallwerke Ghh | Verwendung einer kupferlegierung als werkstoff fuer stranggiesskokillen |
US5435828A (en) * | 1993-12-21 | 1995-07-25 | United Technologies Corporation | Cobalt-boride dispersion-strengthened copper |
JPH0827531A (ja) * | 1994-07-14 | 1996-01-30 | Sumitomo Electric Ind Ltd | 銅合金導体およびその製造方法 |
JPH08174272A (ja) * | 1994-12-21 | 1996-07-09 | Mitsui Mining & Smelting Co Ltd | 硬化肉盛用銅基合金粉末 |
JPH10158766A (ja) * | 1996-11-29 | 1998-06-16 | Miyoshi Gokin Kogyo Kk | 耐熱・耐摩耗性銅合金 |
-
2003
- 2003-04-30 JP JP2003124746A patent/JP4360832B2/ja not_active Expired - Lifetime
-
2004
- 2004-04-23 US US10/829,946 patent/US20040261913A1/en not_active Abandoned
- 2004-04-26 AT AT04009838T patent/ATE456681T1/de not_active IP Right Cessation
- 2004-04-26 DE DE602004025310T patent/DE602004025310D1/de not_active Expired - Lifetime
- 2004-04-26 EP EP04009838A patent/EP1473374B1/fr not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
ATE456681T1 (de) | 2010-02-15 |
DE602004025310D1 (de) | 2010-03-18 |
JP4360832B2 (ja) | 2009-11-11 |
EP1473374A1 (fr) | 2004-11-03 |
JP2004331993A (ja) | 2004-11-25 |
US20040261913A1 (en) | 2004-12-30 |
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