EP4036261A1 - Platte aus reinem kupfer - Google Patents
Platte aus reinem kupfer Download PDFInfo
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- EP4036261A1 EP4036261A1 EP20870402.3A EP20870402A EP4036261A1 EP 4036261 A1 EP4036261 A1 EP 4036261A1 EP 20870402 A EP20870402 A EP 20870402A EP 4036261 A1 EP4036261 A1 EP 4036261A1
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- grain boundary
- copper plate
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- 239000010949 copper Substances 0.000 title claims abstract description 143
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 130
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 127
- 239000013078 crystal Substances 0.000 claims abstract description 181
- 238000005259 measurement Methods 0.000 claims description 89
- 238000010438 heat treatment Methods 0.000 claims description 75
- 238000000034 method Methods 0.000 claims description 32
- 238000001887 electron backscatter diffraction Methods 0.000 claims description 28
- 239000011159 matrix material Substances 0.000 claims description 24
- 229910052711 selenium Inorganic materials 0.000 claims description 19
- 229910052714 tellurium Inorganic materials 0.000 claims description 19
- 238000005096 rolling process Methods 0.000 claims description 18
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- 229910052790 beryllium Inorganic materials 0.000 claims description 16
- 229910052793 cadmium Inorganic materials 0.000 claims description 16
- 229910052804 chromium Inorganic materials 0.000 claims description 16
- 229910052742 iron Inorganic materials 0.000 claims description 16
- 229910052745 lead Inorganic materials 0.000 claims description 16
- 229910052749 magnesium Inorganic materials 0.000 claims description 16
- 229910052759 nickel Inorganic materials 0.000 claims description 16
- 229910052698 phosphorus Inorganic materials 0.000 claims description 16
- 229910052718 tin Inorganic materials 0.000 claims description 16
- 229910052788 barium Inorganic materials 0.000 claims description 14
- 229910052735 hafnium Inorganic materials 0.000 claims description 14
- 229910052712 strontium Inorganic materials 0.000 claims description 14
- 229910052719 titanium Inorganic materials 0.000 claims description 14
- 229910052727 yttrium Inorganic materials 0.000 claims description 14
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- 230000001629 suppression Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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- 238000003825 pressing Methods 0.000 description 1
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- 238000012795 verification Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
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- 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
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
- C22C1/03—Making non-ferrous alloys by melting using master alloys
-
- 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
Definitions
- the present invention relates to a pure copper plate or sheet suitable as electric or electronic components such as a heat sink, a thick copper circuit, or the like and particularly the present invention relates to a pure copper plate or sheet in which coarsening of crystal grains during being heated is suppressed.
- copper or a copper alloy with excellent electrical conductivity has been used for electric or electronic components such as a heat sink, a thick copper circuit, or the like.
- an insulating circuit substrate or the like in which a copper plate or sheet material is bonded to a ceramic substrate and the copper plate or sheet material is provided as the heat sink or the thick copper circuit has been used.
- the bonding temperature is frequently set to 800°C or higher, and there is a concern that the crystal grains of the copper material constituting the heat sink or the thick copper circuit may be coarsened during the bonding.
- crystal grains tend to be coarsened.
- the burr height increases as the thickness of the plate or sheet increases.
- the coarsening of the crystal grains may cause a problem in appearance.
- Patent Document 1 suggests a pure copper plate or sheet material in which the growth of crystal grains is suppressed.
- Patent Document 1 describes that in a case where the copper plate or sheet contains 0.0006 to 0.0015 wt% of S, crystal grains can be adjusted to have a certain size even when subjected to a heat treatment at a temperature of a recrystallization temperature or higher.
- Patent Document 1 the coarsening of crystal grains is suppressed by specifying the amount of S, but the effect of suppressing coarsening of crystal grains cannot be sufficiently obtained only by specifying the amount of S depending on the heat treatment conditions.
- the crystal grains are locally coarsened, and this results in non-uniformity of the crystal structure in some cases.
- Patent Document 1 Japanese Unexamined Patent Application, First Publication No. H06-002058
- the present invention has been made in consideration of the above-described circumstances, and an object thereof is to provide a pure copper plate or sheet which has high electrical conductivity and is capable of suppressing coarsening and non-uniformity of crystal grains even after a heat treatment.
- suppression of the growth of crystal grains has the same definition as suppression of the coarsening of crystal grains.
- a pure copper plate or sheet including: 99.96% by mass or greater of Cu, in which when an average crystal grain size of crystal grains in a rolled surface is represented by X ⁇ m and an amount of Ag is represented by Y mass ppm, a relational expression of 1 ⁇ 10 -8 ⁇ X -3 Y -1 ⁇ 1 ⁇ 10 -5 is satisfied, and in which a surface orthogonal to a rolling width direction is used as an observation surface, measurement regarding a matrix is performed on a measurement area of 10000 ⁇ m 2 or greater at every measurement intervals of 0.25 ⁇ m by an EBSD method, measured results are analyzed by data analysis software OIM to obtain a CI value in each measurement point, a measurement point in which a CI value is 0.1 or less is removed, an orientation difference between crystal grains is analyzed, a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain
- the EBSD method denotes an electron backscatter diffraction patterns (EBSD) method using a scanning electron microscope provided with a backscattered electron diffraction image system
- the OIM denotes data analysis software (orientation imaging microscopy: OIM) for analyzing crystal orientation using data measured by EBSD
- the CI value denotes a confidence index, which is a numerical value displayed as a numerical value showing the reliability of crystal orientation determination when analyzed using analysis software OIM Analysis (Ver. 7.3.1) of an EBSD device (for example, "EBSD Reader: Using OIM (Revised 3rd Edition)" written by Seiichi Suzuki, September 2009, published by TSL Solutions Inc.).
- the crystal pattern is not clear; and therefore, the reliability of crystal orientation determination is lowered, and the CI value is lowered.
- the CI value is 0.1 or less, it is determined that the structure of the measurement point is a deformed structure.
- the special grain boundary is defined as a coincidence boundary in which a ⁇ value satisfies a relationship of 3 ⁇ ⁇ ⁇ 29, and the ⁇ value is crystallographically defined based on CSL theory ( Kronberg et al: Trans. Met. Soc. AIME, 185, 501 (1949 )), and the coincidence boundary is a grain boundary in which the intrinsic corresponding site lattice orientation defect Dq satisfies a relationship of Dq ⁇ 15°/ ⁇ 1/2 ( D. G. Brandon: Acta. Metallurgica. Vol. 14, p. 1479, (1966 )).
- the random grain boundary is a grain boundary other than the special grain boundary having a coincidence orientation relationship in which a ⁇ value is 29 or less and satisfies Dq ⁇ 15°/ ⁇ 1/2 . That is, the special grain boundary has a coincidence orientation relationship in which a ⁇ value is 29 or less and satisfies Dq ⁇ 15°/ ⁇ 1/2 , and the grain boundary other than the special grain boundary is the random grain boundary.
- grain boundary triple junctions four kinds of grain boundary triple junctions, J0 where all three grain boundaries are random grain boundaries, J1 where one grain boundary is a special grain boundary and two grain boundaries are random grain boundaries, J2 where two grain boundaries are special grain boundaries and one grain boundary is a random grain boundary, and J3 where all three grain boundaries are special grain boundaries, are present.
- the amount of Cu is set to 99.96% by mass or greater, and when the average crystal grain size of the crystal grains on the rolled surface is represented by X ( ⁇ m) and the amount of Ag is represented by Y (mass ppm), an expression of 1 ⁇ 10 -8 ⁇ X -3 Y -1 ⁇ 1 ⁇ 10 -5 is satisfied. Therefore, since a part of Ag is segregated at the grain boundaries, the grain boundary energy is lowered due to the segregation, and thus the coarsening of the crystal grains can be suppressed. In addition, the electrical conductivity of the pure copper plate or sheet can be ensured, and thus the pure copper plate or sheet can be used as the material of a member for electric or electronic devices used for high-current applications and a member for heat dissipation.
- a surface orthogonal to a rolling width direction is used as an observation surface, measurement regarding a matrix is performed on a measurement area of 10000 ⁇ m 2 or greater at every measurement intervals of 0.25 ⁇ m by an EBSD method.
- the measured results are analyzed by data analysis software OIM to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the average grain size A is obtained by Area Fraction.
- Measurement regarding the matrix is performed at every measurement intervals which are 1/10 or less of the average grain size A by the EBSD method.
- the measured results are analyzed by the data analysis software OIM with a total measurement area of 10000 ⁇ m 2 or greater in a plurality of visual fields such that a total of 1000 or more crystal grains are included to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the coincidence boundary with ⁇ 29 or less is defined as a special grain boundary, and the other grain boundaries are defined as random grain boundaries.
- the ratio of J3, where all three grain boundaries constituting a grain boundary triple junction are special grain boundaries, to all grain boundary triple junctions is defined as NF J3 and the ratio of J2, where two grain boundaries constituting a grain boundary triple junction are special grain boundaries and one grain boundary constituting the grain boundary triple junction is a random grain boundary, to all grain boundary triple junctions is defined as NF J2 .
- the pure copper plate or sheet according to one aspect of the present invention since an expression of 0.30 ⁇ (NF J2 /(1- NF J3 )) 0.5 ⁇ 0.48 is satisfied and the grain boundary network is formed of special grain boundaries with low energy, the driving force for recrystallization during heating is small, and the grain growth can be suppressed.
- a total amount of Mg and Sn is set to be in a range of 0.1 mass ppm or greater and 100 mass ppm or less.
- the pure copper plate or sheet contains Mg and Sn at a total amount of 0.1 mass ppm or greater, and Mg and Sn correspond to the elements that suppress the growth of crystal grains, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment. Further, the electrical conductivity can be sufficiently ensured by limiting the total amount of Mg and Sn to 100 mass ppm or less.
- an amount of S is set to be in a range of 1 mass ppm or greater and 20 mass ppm or less.
- the pure copper plate or sheet contains 1 mass ppm or greater of S corresponding to the element that suppresses the growth of crystal grains, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment. Further, the hot workability can be sufficiently ensured by limiting the amount of S to 20 mass ppm or less.
- a total amount of Pb, Se, and Te is 0.3 mass ppm or greater and 10 mass ppm or less.
- Pb, Se, and Te which may be contained as inevitable impurities, are elements that are segregated at the crystal grain boundaries and suppress the coarsening of the crystal grains. Therefore, in a case where the pure copper plate or sheet contains these elements at a total amount of 0.3 mass ppm or greater, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment. Further, in a case where a large amount of these elements are present, the elements also have an effect of suppressing segregation at the grain boundaries of Ag, and thus the hot workability is lowered. Therefore, in a case where the total amount of Pb, Se, and Te is set to 10 mass ppm or less, the effect of suppressing the grain growth can be sufficiently exhibited without impairing the effect of Ag.
- a total amount of Sr, Ba, Ti, Zr, Hf, and Y is 10 mass ppm or less.
- Sr, Ba, Ti, Zr, Hf, and Y may be contained as inevitable impurities, and there is a concern that these elements are segregated at the crystal grain boundaries to prevent the segregation of Ag, and these elements generates compounds with elements (S, Se, Te, and the like) that suppress the coarsening of the crystal grains to impair the effect of elements that suppress the coarsening of the crystal grains. Therefore, the effect of the elements that suppress the growth of crystal grains (the effect of suppressing the growth of crystal grains) can be sufficiently exhibited by limiting the total amount of Sr, Ba, Ti, Zr, Hf, and Y to 10 mass ppm or less, and thus the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment.
- a total amount of Al, Cr, P, Be, Cd, Ni, and Fe is 0.3 mass ppm or greater and 10 mass ppm or less.
- the elements such as Al, Cr, P, Be, Cd, Ni, and Fe, which may be contained as inevitable impurities, have an effect of suppressing the grain growth due to solid solution in the copper matrix, segregation at the grain boundaries, and formation of oxides. Therefore, in a case where the pure copper plate or sheet contains these elements at a total amount of 0.3 mass ppm or greater, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment. Further, in a case where a large amount of such elements are present, there is a concern that these elements are segregated at the crystal grain boundaries to prevent the segregation of Ag.
- the effect of the elements that suppress the growth of crystal grains can be sufficiently exhibited by limiting the total amount of Al, Cr, P, Be, Cd, Ni, and Fe to 10 mass ppm or less, and thus the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment.
- a ratio d max /d ave of a maximum crystal grain size d max to an average crystal grain size d ave in a range of 50 mm ⁇ 50 mm after a heat treatment maintained at 800°C for 1 hour is 20 or less, and the average crystal grain size d ave is 400 ⁇ m or less.
- a Vickers hardness is 150 Hv or less.
- the pure copper plate or sheet is sufficiently soft, and the characteristics as a pure copper plate or sheet are ensured, the pure copper plate or sheet is particularly suitable as a material for electric or electronic components used for high-current applications.
- a pure copper plate or sheet that has high electrical conductivity and is capable of suppressing coarsening and non-uniformity of crystal grains even after a heat treatment.
- Fig. 1 is a flow chart showing a method for producing a pure copper plate or sheet according to the present embodiment.
- the pure copper plate or sheet according to the present embodiment is used as a material for electric or electronic components such as a heat sink or a thick copper circuit and is used by being bonded to, for example, a ceramic substrate in a case of forming the above-described electric or electronic components.
- the pure copper plate or sheet according to the present embodiment contains 99.96% by mass or greater of Cu, and when the average crystal grain size of crystal grains in a rolled surface is represented by X ( ⁇ m) and the amount of Ag is represented by Y (mass ppm), the following relational expression is satisfied. 1 ⁇ 10 ⁇ 8 ⁇ X ⁇ 3 ⁇ Y ⁇ 1 ⁇ 1 ⁇ 10 ⁇ 5
- a surface orthogonal to a rolling width direction is used as an observation surface, measurement regarding a matrix is performed on a measurement area of 10000 ⁇ m 2 or greater at every measurement intervals of 0.25 ⁇ m by an EBSD method.
- the measured results are analyzed by data analysis software OIM to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the average grain size A is acquired by Area Fraction using the data analysis software OIM.
- the measurement regarding the matrix is performed at every measurement intervals which are 1/10 or less of the average grain size A by the EBSD method.
- the measured results are analyzed by the data analysis software OIM with a total measurement area of 10000 ⁇ m 2 or greater in a plurality of visual fields such that a total of 1000 or more crystal grains are included to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the coincidence boundary with ⁇ 29 or less is defined as a special grain boundary, and the other grain boundaries are defined as random grain boundaries.
- the matrix is measured twice by the EBSD method.
- the average grain size A is obtained.
- the measurement interval in the second measurement is determined by the obtained average grain size A.
- the total amount of Mg and Sn is set to be in a range of 0.1 mass ppm or greater and 100 mass ppm or less.
- the amount of S is in set to be in a range of 1 mass ppm or greater and 20 mass ppm or less.
- the total amount of Pb, Se, and Te is 0.3 mass ppm or greater and 10 mass ppm or less.
- the total amount of Sr, Ba, Ti, Zr, Hf, Y (A element group) is 10 mass ppm or less.
- the total amount of Al, Cr, P, Be, Cd, Ni, and Fe (M element group) is 0.3 mass ppm or greater and 10 mass or less.
- composition of the pure copper plate or sheet can also be described as follows.
- the pure copper plate or sheet contains 99.96% by mass or greater of Cu, and Ag, with the balance being inevitable impurities.
- the pure copper plate or sheet further contains either one or both of Mg and Sn in a total amount of 0.1 mass ppm or greater and 100 mass ppm or less.
- the pure copper plate or sheet further contains 1 mass ppm or greater and 20 mass ppm or less of S.
- the pure copper plate or sheet further contains one or more selected from Pb, Se, and Te in a total amount of 0.3 mass ppm or greater and 10 mass ppm or less.
- the pure copper plate or sheet further contains at least one selected from Sr, Ba, Ti, Zr, Hf, and Y in a total amount of 10 mass ppm or less.
- the pure copper plate or sheet further contains one or more selected from Al, Cr, P, Be, Cd, Ni, and Fe in a total amount of 0.3 mass ppm or greater and 10 mass ppm or less.
- the preferable ranges of the amounts thereof are as described above even in a case where the pure copper plate or sheet contains the elements as inevitable impurities or intentionally. Further, it can also be said that the elements other than Cu are inevitable impurities. It can also be said that the inevitable impurities as the balance are elements other than the elements whose amounts are specified above.
- a ratio d max /d ave of a maximum crystal grain size d max to an average crystal grain size d ave in a range of 50 mm ⁇ 50 mm after a heat treatment maintained at 800°C for 1 hour is 20 or less and the average crystal grain size d ave is 400 ⁇ m or less.
- the Vickers hardness is preferably 150 Hv or less.
- the electrical conductivity is 97% IACS or greater.
- the electric or electronic component for high-current applications is required to have excellent electrical conductivity and heat dissipation in order to suppress heat generation during electrical conduction, and pure copper with particularly excellent electrical conductivity and heat dissipation is preferably used. Further, in a case where the component is bonded to a ceramic substrate or the like, it is preferable that the deformation resistance is small so that the thermal strain generated during a thermal cycle can be mitigated.
- the purity of Cu is specified to 99.96% by mass or greater.
- the purity of Cu is preferably 99.965% by mass or greater and more preferably 99.97% by mass or greater.
- the upper limit of the purity of Cu is not particularly limited, but in a case where the purity thereof is greater than 99.9999% by mass, a special refining step is required, and the production cost significantly increases. Therefore, the upper limit thereof is preferably set to 99.9999% by mass or less.
- Ag has a narrow solid solution limit at a low temperature and thus Ag is unlikely to be dissolved into the Cu matrix. Therefore, a part of Ag that is dissolved into the matrix is segregated at the grain boundaries by performing the heat treatment at a high temperature so that Ag is dissolved into copper (the Cu matrix) and performing warm working at a temperature of 150°C or higher and 350°C or lower. As a result, the grain boundary energy is decreased, the coarsening of a part of crystal grains during being heated at a high temperature and abnormal grain growth due to secondary recrystallization are suppressed, and thus uniformity of the crystal grain size can be realized.
- the average crystal grain size of the crystal grains in the rolled surface is represented by X ⁇ m and the amount of Ag is represented by Y mass ppm
- the amount of Ag is small and the average crystal grain size is small in some cases when the value of X -3 Y -1 is large. Therefore, the grain boundary area contained per unit volume increases, and Ag cannot be sufficiently segregated at the grain boundaries. Therefore, the crystal grains are coarsened when heated at a high temperature, and the variation in grain size increases.
- the amount of Ag is large and the average crystal grain size is large in some cases when the value of X -3 Y -1 is small.
- the effect of suppressing the grain growth is high, but the amount of expensive Ag is large, and the heat treatment temperature is high for a long time, and thus this results in a significant cost increase.
- the upper limit of X -3 Y -1 is preferably 7.5 ⁇ 10 -6 or less, more preferably 5.0 ⁇ 10 -6 or less, and still more preferably 3.0 ⁇ 10 -6 or less, and most preferably 2.0 ⁇ 10 -6 or less. Further, the lower limit of X -3 Y -1 is preferably 5.0 ⁇ 10 -8 or greater and more preferably 1.0 ⁇ 10 -7 or greater.
- the substantial amount of Ag to be added is 5 mass ppm or greater and 150 mass ppm or less.
- the amount of Ag is less than 5 mass ppm, the grain size is required to be further increased, which may cause a problem of a cost increase as well as a problem of poor appearance due to the relative increase in grain size after the heat treatment. Therefore, the substantial lower limit of Ag is 5 mass ppm or greater.
- the lower limit is preferably 6 mass ppm or greater and more preferably 7 mass ppm or greater.
- the substantial upper limit thereof is 150 mass ppm or less.
- the upper limit thereof is preferably 100 mass ppm or less, more preferably 60 mass ppm or less, still more preferably 50 mass ppm or less, even still more preferably 40 mass ppm or less, even still more preferably 30 mass ppm or less, and most preferably 25 mass ppm or less.
- the crystal grain growth when the pure copper plate or sheet is subjected to a heat treatment at a high temperature is due to a high grain boundary movement speed of random grain boundaries with high grain boundary energy. Accordingly, by forming two or three of the three grain boundaries constituting a grain boundary triple junction into special grain boundaries with low grain boundary energy represented by ⁇ 29 or less, grain growth at a high temperature is suppressed and the uniformity of the crystal grain size can be realized.
- a surface orthogonal to a rolling width direction is used as an observation surface, measurement regarding a matrix is performed on a measurement area of 10000 ⁇ m 2 or greater at every measurement intervals of 0.25 ⁇ m by an EBSD method.
- the measured results are analyzed by data analysis software OIM to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the average grain size A is obtained by Area Fraction.
- the measurement regarding the matrix is performed at every measurement intervals which are 1/10 or less of the average grain size A by the EBSD method.
- the measured results are analyzed by the data analysis software OIM with a total measurement area of 10000 ⁇ m 2 or greater in a plurality of visual fields such that a total of 1000 or more crystal grains are included to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the coincidence boundary with ⁇ 29 or less is defined as a special grain boundary, and the other grain boundaries are defined as random grain boundaries.
- (NF J2 /(1-NF J3 )) 0-5 is set to be greater than 0.30 and 0.48 or less.
- the upper limit of (NF J2 /(1-NF J3 )) 0.5 is preferably 0.47 or less and more preferably 0.46 or less. Further, the lower limit of (NF J2 /(1-NF J3 )) 0.5 is preferably greater than 0.31 and more preferably greater than 0.32.
- NF J2 increases as NF J3 increases. Therefore, NF J3 is preferably 0.007 or greater, more preferably 0.008 or greater, and still more preferably 0.010 or greater. Further, in order to suppress the burr height, NF J3 is preferably 0.036 or less, more preferably 0.034 or less, and still more preferably 0.030 or less.
- Total amount of Mg and Sn 0.1 mass ppm or greater and 100 mass ppm or less
- Mg and Sn are elements having an effect of suppressing coarsening of crystal grains by being dissolved into the matrix of copper. Therefore, in a case where the total amount of Mg and Sn is set to 0.1 mass ppm or greater in the present embodiment, the effect of suppressing the coarsening of crystal grains using Mg and Sn can be exhibited, and the coarsening of crystal grains can be reliably suppressed even after the heat treatment. Meanwhile, since there is a concern of an increase in the production cost and a decrease in the electrical conductivity due to the addition more than necessary, the amount of either one or both of Mg and Sn is set to less than 100 mass ppm.
- the lower limit of the amount of either one or both of Mg and Sn is set to preferably 0.5 mass ppm or greater and more preferably 1 mass ppm or greater. Further, the upper limit of the total amount of Mg and Sn is preferably less than 80 mass ppm, more preferably less than 60 mass ppm, and most preferably less than 10 mass ppm.
- S is an element that has an effect of suppressing coarsening of crystal grains by suppressing movement of crystal grain boundaries and lowers hot workability.
- the amount of S is set to 1 mass ppm or more in the present embodiment, the effect of suppressing the coarsening of the crystal grains due to S can be sufficiently exhibited, and the coarsening of the crystal grains can be reliably suppressed even after the heat treatment. Further, in a case where the amount of S is limited to 20 mass ppm or less, the hot workability can be ensured.
- the lower limit of the amount of S is preferably 2 mass ppm or greater and more preferably 3 mass ppm or greater. Further, the upper limit of the amount of S is preferably 17.5 mass ppm or less and more preferably 15 mass ppm or less.
- Total amount of Pb, Se, and Te 0.3 mass ppm or greater and 10 mass ppm or less
- Pb, Se, and Te have a low solid solution limit in Cu and have an effect of suppressing coarsening of the crystal grains by being segregated at grain boundaries. Further, Pb, Se and Te are elements that also have an effect of suppressing segregation of Ag at grain boundaries by existing in a large amount and lower the hot workability.
- the total amount of Pb, Se, and Te it is preferable to limit the total amount of Pb, Se, and Te to 10 mass ppm or less in order to exhibit the effect of suppressing coarsening and to ensure hot workability at the same time.
- the lower limit of the total amount of Pb, Se, and Te is preferably set to 0.3 mass ppm or greater.
- the upper limit of the total amount of Pb, Se, and Te is set to preferably 9 mass ppm or less, more preferably 8 mass ppm or less, and still more preferably 7 mass ppm or less. Further, the lower limit of the total amount of Pb, Se, and Te is set to preferably 0.4 mass ppm or greater and more preferably 0.5 mass ppm or greater.
- Total amount of Sr, Ba, Ti, Zr, Hf, and Y 10 mass ppm or less
- Sr, Ba, Ti, Zr, Hf, and Y (A element group) contained as inevitable impurities are segregated at the crystal grain boundaries to generate compounds with elements (S, Se, Te, and the like) that suppress the coarsening of the crystal grains and thus may impair the effect of elements that suppress the coarsening of the crystal grains.
- the total amount of Sr, Ba, Ti, Zr, Hf, and Y is set to 10 mass ppm or less.
- the total amount of Sr, Ba, Ti, Zr, Hf, and Y (A element group) is preferably 7.5 mass ppm or less and more preferably 5 mass ppm or less.
- the lower limit is not particularly specified, but the cost may increase due to refining in a case where the total amount of Sr, Ba, Ti, Zr, Hf, and Y (A element group) is less than 0.01 mass ppm, and thus the total amount of Sr, Ba, Ti., Zr, Hf, and Y (A element group) is preferably 0.01 mass ppm or greater and more preferably 0.05 mass ppm or greater.
- Total amount of Al, Cr, P, Be, Cd, Ni, and Fe (M element group): 0.3 mass ppm or greater and 10 mass or less)
- Al, Cr, P, Be, Cd, Ni, and Fe have an effect of suppressing grain growth by being dissolved into the matrix of copper, being segregated at grain boundaries, and forming oxides.
- the total amount of Al, Cr, P, Be, Cd, Ni, and Fe (M element group) is preferably set to 0.3 mass ppm or greater.
- the lower limit of the total amount of Al, Cr, P, Be, Cd, Ni, and Fe (M element group) is set to more preferably 1.0 mass ppm or greater, still more preferably 1.5 mass ppm or greater, even still more preferably 2.0 mass ppm or greater, and most preferably 2.5 mass ppm or greater.
- the upper limit of the total amount of Al, Cr, P, Be, Cd, Ni, and Fe (M element group) is set to preferably 10 mass ppm or less, more preferably less than 8 mass ppm, and still more preferably less than 5 mass ppm.
- Examples of inevitable impurities other than the above-described elements include B, Bi, Ca, Sc, rare earth elements, V, Nb, Ta, Mo, W, Mn, Re, Ru, Os, Co, Rh, Ir, Pd, Pt, Au, Zn, Hg, Ga, In, Ge, As, Sb, Tl, N, C, Si, Li, H, and O. Since these inevitable impurities may decrease the electrical conductivity, it is preferable that the amount thereof is as small as possible.
- the pure copper plate or sheet according to the present embodiment in a case where the average crystal grain size after heat treatment maintained at 800°C for 1 hour is 400 ⁇ m or less, since the coarsening of crystal grains can be reliably suppressed even when the pure copper plate or sheet is heated at a temperature of 800°C or higher, the pure copper plate or sheet is particularly suitable as a material for a thick copper circuit and a heat sink to be bonded to a ceramic substrate.
- the upper limit of the average crystal grain size after the heat treatment maintained at 800°C for 1 hour is preferably 380 ⁇ m or less and more preferably 350 ⁇ m or less.
- the lower limit of the average crystal grain size after the heat treatment maintained at 800°C for 1 hour is not particularly limited, but is usually 200 ⁇ m or greater.
- the pure copper plate or sheet according to the present embodiment in a case where the ratio d max /d ave of the maximum crystal grain size d max to the average crystal grain size d ave in a range of 50 mm ⁇ 50 mm after the heat treatment maintained at 800°C for 1 hour is 20 or less, since the non-uniformity of crystal grains can be reliably suppressed even when the pure copper plate or sheet is heated at 800°C or higher, the pure copper plate or sheet is particularly suitable as a material for a thick copper circuit and a heat sink to be bonded to a ceramic substrate.
- the ratio d max /d ave of the maximum crystal grain size d max to the average crystal grain size d ave in a range of 50 mm ⁇ 50 mm after the heat treatment maintained at 800°C for 1 hour is preferably 18 or less and more preferably 16 or less.
- the pure copper plate or sheet in a case where the Vickers hardness is set to 150 Hv or less, the characteristics as a pure copper plate or sheet are ensured, and thus the pure copper plate or sheet is particularly suitable as a material for electric or electronic components for high-current applications. Further, since the pure copper plate or sheet is sufficiently soft, the thermal strain generated by the deformation of the pure copper plate or sheet can be released even in a case where the pure copper plate or sheet is bonded to another member such as a ceramic substrate and a thermal cycle is loaded.
- the Vickers hardness is preferably 140 Hv or less, more preferably 120 Hv or less, still more preferably 100 Hv or less, and even still more preferably 95 Hv or less.
- the lower limit of the Vickers hardness is not particularly limited, but is preferably 60 Hv or greater.
- the pure copper plate or sheet in a case where the electrical conductivity is set to 97% IACS or greater, the characteristics as a pure copper plate or sheet are ensured, and thus the pure copper plate or sheet is particularly suitable as a material of a member for electric or electronic devices used for high-current applications and a member for heat dissipation.
- the electrical conductivity is preferably 98% IACS or greater, more preferably 99% IACS or greater, and even still more preferably 100% IACS or greater.
- the upper limit of the electrical conductivity is not particularly limited, but is usually 103% IACS or less.
- the above-described elements are added to molten copper obtained by melting the copper raw material to adjust components; and thereby, a molten copper alloy is produced.
- a single element, a base alloy, or the like can be used for addition of various elements.
- raw materials containing the above-described elements may be melted together with the copper raw material.
- a recycled material or a scrap material of the alloy according to the present embodiment may be used.
- the molten copper so-called 4 NCu having a purity of 99.99% by mass or greater or so-called 5 NCu having a purity of 99.999% by mass or greater is preferably used.
- atmosphere-controlled melting is performed using an inert gas atmosphere (for example, Ar gas or N2 gas) in which the vapor pressure of H 2 O is low and the holding time during melting is set to the minimum.
- an inert gas atmosphere for example, Ar gas or N2 gas
- the molten copper alloy in which the components have been adjusted is injected into a mold to produce an ingot.
- the cooling rate of the molten metal is set to preferably 0.1 °C/sec or greater and more preferably 0.5°C/sec or greater.
- the hot working temperature is not particularly limited, but is preferably set to be in a range of 500°C or higher and 1000°C or lower.
- the total working rate of hot working is preferably 50% or greater, more preferably 60% or greater, and still more preferably 70% or greater.
- a cooling method after the hot working is not particularly limited, but it is preferable to perform air cooling or water cooling.
- the working method in the hot working step S02 is not particularly limited, and examples of the method which can be employed include rolling, extruding, groove rolling, forging, and pressing.
- warm working is carried out at a temperature of 150°C or higher and 350°C or lower.
- Ag can be segregated in the vicinity of the grain boundaries, and the grain boundary energy can be lowered.
- warm working may be combined with cold working.
- warm working may be performed in a plurality of passes before the final working. For example, in a case of rolling, the final 3 or more passes may be defined as warm working.
- the grain size of the recrystallized grains is preferably 10 ⁇ m or greater. In a case where the recrystallized grains are fine, the growth of the crystal grains and the non-uniformity of the structure may be promoted when the recrystallized grains are subsequently heated to a temperature of 800°C or higher.
- the crystal grain size after recrystallization is preferably 15 ⁇ m or greater, more preferably 20 ⁇ m or greater, and still more preferably 25 ⁇ m or greater.
- the heat treatment conditions in the recrystallization heat treatment step S04 are not particularly limited, but it is preferable that the heat treatment is performed at a heat treatment temperature of 200°C or higher and 900°C or lower for a holding time of 1 second or longer and 10 hours or shorter.
- the rough working step S03 and the recrystallization heat treatment step S04 may be repeatedly performed two or more times.
- the copper material after the recrystallization heat treatment step S04 may be subjected to temper deforming.
- the working rate of the temper deforming is not particularly limited, but it is preferable that the temper deforming is performed at a working rate of greater than 0% and 50% or less in order to adjust the strength of the material. It is more preferable to limit the working rate to 3% or greater and 40% or less.
- the heat treatment may be further performed after the temper deforming in order to remove the residual strain.
- the pure copper plate or sheet according to the present embodiment is produced.
- the pure copper plate or sheet of the present embodiment with the above-described configuration, when the average crystal grain size of the crystal grains in the rolled surface is represented by X ( ⁇ m) and the amount of Ag is represented by Y (mass ppm), a relational expression of 1 ⁇ 10 -8 ⁇ X -3 Y -1 ⁇ 1 ⁇ 10 -5 is satisfied. Therefore, a part of Ag is segregated at the grain boundaries to reduce the grain boundary energy, and thus the coarsening of the crystal grains can be suppressed.
- a surface orthogonal to a rolling width direction is used as an observation surface, measurement regarding a matrix is performed on a measurement area of 10000 ⁇ m 2 or greater at every measurement intervals of 0.25 ⁇ m by an EBSD method.
- the measured results are analyzed by data analysis software OIM to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the average grain size A is obtained by Area Fraction.
- the measurement regarding the matrix is performed at every measurement intervals which are 1/10 or less of the average grain size A by the EBSD method.
- the measured results are analyzed by the data analysis software OIM with a total measurement area of 10000 ⁇ m 2 or greater in a plurality of visual fields such that a total of 1000 or more crystal grains are included to obtain a CI value in each measurement point.
- the measurement point in which a CI value is 0.1 or less is removed.
- the orientation difference between crystal grains is analyzed by the data analysis software OIM, and a boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the coincidence boundary with ⁇ 29 or less is defined as a special grain boundary, and the other grain boundaries are defined as random grain boundaries.
- the amount of Mg and Sn corresponding to the elements that suppress the growth of crystal grains is 0.1 mass ppm or greater, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment. Further, in a case where the total amount of Mg and Sn is limited to 100 mass ppm or less, the electrical conductivity can be sufficiently ensured.
- the amount of S is set to be in a range of 1 mass ppm or greater and 20 mass ppm or less
- S which is a kind of element that suppresses the growth of crystal grains, is segregated at the grain boundaries, and the coarsening and non-uniformity of the crystal grains during heating can be reliably suppressed.
- the hot workability can be ensured.
- the total amount of Pb, Se, and Te which are elements that are segregated at the crystal grain boundaries to suppress the coarsening of the crystal grains, is set to 0.3 mass ppm or greater, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment.
- the total amount of Pb, Se, and Te is set to 10 mass ppm or less, the effect of suppressing the grain growth can be sufficiently exhibited without impairing the effect of Ag.
- the elements of the A element group do not impair the effect of Ag which is an element that suppresses the growth of crystal grains and can suppress reaction of the elements in the A element group with S, Se, Te, and the like to generate compounds. Therefore, the effect of the elements that suppress the growth of crystal grains can be sufficiently exhibited. Therefore, the coarsening and non-uniformity of the crystal grains during heating can be reliably suppressed.
- the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment by dissolving into the matrix of copper, segregation at grain boundaries, and formation of oxides.
- the total amount of Al, Cr, P, Be, Cd, Ni, and Fe is limited to 10 mass ppm or less, the effect of suppressing the growth of crystal grains without suppressing the effect of Ag can be sufficiently exhibited, and the coarsening and non-uniformity of the crystal grains during heating can be reliably suppressed.
- the ratio d max /d ave of the maximum crystal grain size d max to the average crystal grain size d ave in a range of 50 mm ⁇ 50 mm after the heat treatment maintained at 800°C for 1 hour is 20 or less and the average crystal grain size d ave is 400 ⁇ m or less, the coarsening and non-uniformity of the crystal grains can be reliably suppressed even after the heat treatment, and the occurrence of poor appearance can be further suppressed.
- the pure copper plate or sheet in a case where the Vickers hardness is 150 Hv or less, since the pure copper plate or sheet is sufficiently soft and the characteristics as a pure copper plate or sheet are ensured, the pure copper plate or sheet is particularly suitable as a material for electric or electronic components for high-current applications.
- the example of the method of producing the pure copper plate or sheet has been described, but the method of producing the pure copper plate or sheet is not limited to the description of the embodiment, and the pure copper plate or sheet may be produced by appropriately selecting a production method of the related art.
- the average crystal grain size X of the crystal grains in the rolled surface, and the maximum crystal grain size d max and the average crystal grain size d ave after the heat treatment maintained at 800°C for 1 hour are measured by the methods described in the following examples.
- a copper raw material formed of pure copper having a purity of 99.999% by mass or greater was prepared, the copper raw material was put into a high-purity graphite crucible, and subjected to high-frequency induction heating in a furnace in which the atmosphere was set to an Ar gas atmosphere so that the material was melted.
- Each element was added to the obtained molten copper and poured into a carbon mold to produce an ingot having the component composition listed in Tables 1 and 3. Thereafter, a part of the ingot was cut and machined to obtain an ingot having a thickness of 50 mm, a width of 100 mm, and a length of 100 mm.
- the ingot was heated in an electric furnace at 800°C for 4 hours in an Ar gas atmosphere and subjected to a homogenization treatment.
- the ingot after the homogenization heat treatment was hot-forged by free forging such that the forging ratio reached 4 or greater to obtain a plate or sheet material having a height of approximately 25 mm and a width of approximately 150 mm.
- the ingot was hot-forged at 500°C or higher, the ingot was reheated in an electric furnace maintained at 800°C when the surface temperature reached 500°C or lower, and the ingot was hot-forged again when the surface temperature reached approximately 600°C.
- the temperature when the hot forging was completed was 500°C or higher.
- a solutionizing heat treatment was performed for 1 minute in an electric furnace heated to 800°C.
- the forged plate or sheet material was subjected to surface grinding to remove the oxide film on the surface.
- the rolling roll was heated to 300°C, and rough rolling (warm rolling) was carried out at the rolling rate listed in the tables.
- the copper plate or sheet material after the warm rolling was subjected to the recrystallization heat treatment at the heat treatment temperature listed in Tables 2 and 4 using an electric furnace to adjust the crystal grain size to 10 ⁇ m or greater and 150 ⁇ m or less.
- Measurement specimens were collected from the obtained ingot, and the amount of each element was measured using a glow discharge mass spectrometer (GD-MS). The measurement was performed at two sites, the center portion of the specimen and the end portion of the specimen in the width direction, and the larger amount was defined as the amount of the sample. The measured results are listed in Tables 1 and 3.
- the crystal grain boundaries (special grain boundaries and random grain boundaries) and the grain boundary triple junctions were measured by an EBSD measuring device and OIM analysis software using a cross section orthogonal to the rolling width direction, that is, a transverse direction (TD) surface as an observation surface.
- Mechanical polishing was performed using waterproof abrasive paper and diamond abrasive grains.
- finish polishing was performed using a colloidal silica solution.
- a boundary having 15° or more of an orientation difference between neighboring measuring points was assigned as a grain boundary.
- the average grain size A was acquired by Area Fraction. Thereafter, measurement regarding the matrix was performed at every measurement intervals which were 1/10 or less of the average grain size A by the EBSD method.
- the measured results were analyzed by the data analysis software OIM with a measurement area where the total area of a plurality of visual fields was 10000 ⁇ m 2 or greater such that a total of 1000 or more crystal grains were included, to obtain a CI value in each measurement point.
- the measurement points in which a CI value was 0.1 or less were removed.
- the orientation difference between crystal grains was analyzed by the data analysis software OIM.
- a boundary having 15° or more of an orientation difference between neighboring measuring points was assigned as a grain boundary. Further, for the three grain boundaries constituting each grain boundary triple junction, the special grain boundary and the random grain boundary were identified by using the CSL sigma value calculated by the Neighboring grid point. The coincidence grain boundaries with greater than ⁇ 29 were regarded as random grain boundaries.
- a plurality of circular holes ( ⁇ 8 mm) were punched out from the strip for characteristic evaluation using a metal die, the burr height was measured, and the press workability was evaluated.
- the clearance of the metal die was set to approximately 3% with respect to the thickness of the plate or sheet, and punching was performed at a punching speed of 50 spm (stroke per minute). The cut surface on the punched hole side was observed, the burr heights at 10 or more points were measured, and the ratio of the burr height to the thickness of the plate or sheet was acquired.
- the Vickers hardness was measured with a test load of 0.98 N in conformity with the micro Vickers hardness test method specified in JIS Z 2244. Further, the rolled surface of the test piece for characteristic evaluation was used as the measurement position. The evaluation results are listed in Tables 5 and 6.
- Test pieces having a width of 10 mm and a length of 60 mm were collected from each strip for characteristic evaluation and the electrical resistance was acquired according to a 4 terminal method. Further, the dimension of each test piece was measured using a micrometer and the volume of the test piece was calculated. In addition, the electrical conductivity was calculated from the measured electrical resistance value and volume. The evaluation results are listed in Tables 5 and 6.
- test pieces were collected such that the longitudinal directions thereof were parallel to the rolling direction of each strip for characteristic evaluation.
- a 20 mm ⁇ 20 mm sample was cut out from the obtained strip for characteristic evaluation, and the average crystal grain size was measured by an electron backscatter diffraction patterns (SEM-EBSD) measuring device.
- SEM-EBSD electron backscatter diffraction patterns
- the rolled surface was mechanically polished using waterproof abrasive paper and diamond abrasive grains.
- finish polishing was performed using a colloidal silica solution.
- measurement regarding the matrix was performed on a measurement area of 10000 ⁇ m 2 or greater at every measurement intervals of 0.25 ⁇ m at an electron beam acceleration voltage of 20 kV by an EBSD method using an EBSD measuring device (Quanta FEG 450, manufactured by FEI, OIM Data Collection, manufactured by EDAX/TSL (currently AMETEK)) and analysis software (OIM Data Analysis ver. 7.3.1, manufactured by EDAX/TSL (currently AMETEK)). The measured results were analyzed by the data analysis software OIM to obtain CI values at each measurement point.
- the measurement points in which a CI value was 0.1 or less were removed.
- the orientation difference between crystal grains was analyzed by the data analysis software OIM. A boundary having 15° or more of an orientation difference between neighboring measuring points is assigned as a grain boundary.
- the average grain size A was acquired by Area Fraction. Thereafter, measurement regarding the matrix was performed at every measurement intervals which were 1/10 or less of the average grain size A by the EBSD method.
- the measured results were analyzed by the data analysis software OIM with a measurement area where the total area of a plurality of visual fields was 10000 ⁇ m 2 or greater such that a total of 1000 or more crystal grains were included, to obtain a CI value in each measurement point.
- the measurement points in which a CI value was 0.1 or less were removed.
- the orientation difference between crystal grains was analyzed by the data analysis software OIM.
- a boundary having 15° or more of an orientation difference between neighboring measuring points was assigned as a large-angle grain boundary, and a boundary having less than 15° of an orientation difference between neighboring measuring points was assigned as a small-angle grain boundary.
- a crystal grain boundary map was created using a large-angle grain boundary, and five line segments having a predetermined length were drawn at predetermined intervals in the longitudinal direction and the transverse direction on the crystal grain boundary map in conformity with the cutting method of JIS H 0501. The number of crystal grains that were completely cut was counted, and the average value of the lengths of the cut grains was calculated as the average crystal grain size before the heat treatment.
- the evaluation results are listed in Tables 5 and 6.
- the average crystal grain size before the heat treatment is also the average crystal grain size X ⁇ m of the crystal grains in the rolled surface.
- the values of X -3 Y -1 in which the average crystal grain size of the crystal grains in the rolled surface was represented by X ⁇ m and the amount of Ag was represented by Y mass ppm were calculated and listed in Tables 5 and 6. In a case where the calculated value is "a ⁇ 10 -b ", the value is described as “aE-b" in Tables 5 and 6. For example, "1.2E-08" denotes "1.2 ⁇ 10 -8 ".
- a 60 mm ⁇ 60 mm sample was cut out from the strip for characteristic evaluation described above and subjected to a heat treatment maintained at 800°C for 1 hour.
- a 50 mm ⁇ 50 mm sample was cut out from this test piece, and the rolled surface was mirror-polished and etched. Thereafter, the surface was imaged with an optical microscope such that the rolling direction was on the side of the photograph.
- the site where the crystal grains were the finest and the field of view of approximately 1 mm 2 or greater was formed with a uniform grain size was selected, and observation and measurement were performed in the field of view of approximately of 1 mm 2 or greater.
- the average value of the major axis and the minor axis of the coarsest crystal grains was defined as the maximum crystal grain size d max , excluding twin crystals in a range of 50 mm ⁇ 50 mm.
- the major axis is the length of the longest line segment among the line segments connecting two points on the grain boundary (contour of the crystal grain), and the minor axis is the length of longest line segment among the line segments cut by the grain boundaries when a line is drawn perpendicularly to the major axis.
- Comparative Example 1 X -3 Y -1 was greater than the range of the present embodiment, the variation in the grain size after the heat treatment was evaluated as "B" (poor), and the grain size after the heat treatment was also greater than 400 ⁇ m.
- the average crystal grain size after the heat treatment was small, and the variation in the grain size was small.
- the electrical conductivity was also 97% IACS or greater.
- the pure copper plate or sheet of the present embodiment can be suitably applied to electric or electronic components such as an insulating circuit substrate provided with a copper plate or sheet material as a heat sink or a thick copper circuit.
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Cited By (2)
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| EP4116449A4 (de) * | 2020-03-06 | 2024-03-20 | Mitsubishi Materials Corporation | Platte aus reinem kupfer, kupfer/keramik-verbundkörper und isoliertes schaltungssubstrat |
| EP4116450A4 (de) * | 2020-03-06 | 2024-03-27 | Mitsubishi Materials Corporation | Reine kupferplatte, kupfer-/keramikverbundkörper und isolierte leiterplatte |
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| JP7243904B2 (ja) * | 2021-07-02 | 2023-03-22 | 三菱マテリアル株式会社 | エッジワイズ曲げ加工用銅条、および、電子・電気機器用部品、バスバー |
| JP7215626B2 (ja) * | 2021-07-02 | 2023-01-31 | 三菱マテリアル株式会社 | エッジワイズ曲げ加工用銅条、および、電子・電気機器用部品、バスバー |
| JP7243903B2 (ja) * | 2021-07-02 | 2023-03-22 | 三菱マテリアル株式会社 | エッジワイズ曲げ加工用銅条、および、電子・電気機器用部品、バスバー |
| TW202308768A (zh) * | 2021-07-02 | 2023-03-01 | 日商三菱綜合材料股份有限公司 | 沿層方向彎曲加工用銅條,以及電子、電氣機器用零件、母線 |
| JP7215627B2 (ja) * | 2021-07-02 | 2023-01-31 | 三菱マテリアル株式会社 | エッジワイズ曲げ加工用銅条、および、電子・電気機器用部品、バスバー |
| TW202319552A (zh) * | 2021-07-02 | 2023-05-16 | 日商三菱綜合材料股份有限公司 | 沿層方向彎曲加工用銅條,以及電子、電氣機器用零件、母線 |
| WO2023277197A1 (ja) * | 2021-07-02 | 2023-01-05 | 三菱マテリアル株式会社 | エッジワイズ曲げ加工用銅条、および、電子・電気機器用部品、バスバー |
| US12597534B2 (en) | 2021-07-02 | 2026-04-07 | Mitsubishi Materials Corporation | Copper strip for edgewise bending, component for electric or electronic device, and bus bar |
| WO2024024909A1 (ja) * | 2022-07-29 | 2024-02-01 | 三菱マテリアル株式会社 | 純銅材、絶縁基板、電子デバイス |
| EP4467675A4 (de) * | 2022-07-29 | 2025-12-24 | Mitsubishi Materials Corp | Reines kupfermaterial, isolierendes substrat und elektronische vorrichtung |
| JP7473066B2 (ja) * | 2022-07-29 | 2024-04-23 | 三菱マテリアル株式会社 | 純銅材、絶縁基板、電子デバイス |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH062058A (ja) | 1992-06-23 | 1994-01-11 | Furukawa Electric Co Ltd:The | 結晶粒成長抑制無酸素銅 |
| CN1425196A (zh) * | 1999-11-24 | 2003-06-18 | 霍尼韦尔国际公司 | 导电互连 |
| JP5499933B2 (ja) * | 2010-01-12 | 2014-05-21 | 三菱マテリアル株式会社 | 電気銅めっき用含リン銅アノード、その製造方法および電気銅めっき方法 |
| JP4869415B2 (ja) * | 2010-02-09 | 2012-02-08 | 三菱伸銅株式会社 | 純銅板の製造方法及び純銅板 |
| JP5143208B2 (ja) * | 2010-10-25 | 2013-02-13 | Jx日鉱日石金属株式会社 | 圧延銅箔、並びにこれを用いた負極集電体、負極板及び二次電池 |
| KR101953412B1 (ko) * | 2011-08-05 | 2019-02-28 | 후루카와 덴키 고교 가부시키가이샤 | 이차전지 집전체용 압연 동박 및 그 제조방법 |
| JP5752536B2 (ja) * | 2011-08-23 | 2015-07-22 | Jx日鉱日石金属株式会社 | 圧延銅箔 |
| JP5826160B2 (ja) * | 2012-04-10 | 2015-12-02 | Jx日鉱日石金属株式会社 | 圧延銅箔、銅張積層板、フレキシブルプリント配線板及びその製造方法 |
| JP5752736B2 (ja) * | 2013-04-08 | 2015-07-22 | 三菱マテリアル株式会社 | スパッタリング用ターゲット |
| JP6296728B2 (ja) * | 2013-09-03 | 2018-03-20 | Jx金属株式会社 | 導電性及び曲げたわみ係数に優れる銅合金板 |
| KR20170132146A (ko) * | 2015-04-01 | 2017-12-01 | 후루카와 덴끼고교 가부시키가이샤 | 평각 압연 동박, 플렉시블 플랫 케이블, 회전 커넥터 및 평각 압연 동박의 제조 방법 |
| JP2019176835A (ja) | 2018-03-30 | 2019-10-17 | 三井化学株式会社 | アミド化合物の製造方法 |
-
2020
- 2020-09-11 JP JP2021507700A patent/JP6973680B2/ja active Active
- 2020-09-11 EP EP20870402.3A patent/EP4036261A4/de not_active Withdrawn
- 2020-09-11 CN CN202080059341.XA patent/CN114269957B/zh active Active
- 2020-09-11 KR KR1020227005974A patent/KR20220068985A/ko not_active Ceased
- 2020-09-11 US US17/762,267 patent/US20220403484A1/en active Pending
- 2020-09-11 WO PCT/JP2020/034462 patent/WO2021060023A1/ja not_active Ceased
- 2020-09-24 TW TW109133046A patent/TW202115264A/zh unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4116449A4 (de) * | 2020-03-06 | 2024-03-20 | Mitsubishi Materials Corporation | Platte aus reinem kupfer, kupfer/keramik-verbundkörper und isoliertes schaltungssubstrat |
| EP4116450A4 (de) * | 2020-03-06 | 2024-03-27 | Mitsubishi Materials Corporation | Reine kupferplatte, kupfer-/keramikverbundkörper und isolierte leiterplatte |
| US12035469B2 (en) | 2020-03-06 | 2024-07-09 | Mitsubishi Materials Corporation | Pure copper plate, copper/ceramic bonded body, and insulated circuit board |
Also Published As
| Publication number | Publication date |
|---|---|
| TW202115264A (zh) | 2021-04-16 |
| JP6973680B2 (ja) | 2021-12-01 |
| WO2021060023A1 (ja) | 2021-04-01 |
| JPWO2021060023A1 (ja) | 2021-11-04 |
| CN114269957B (zh) | 2022-07-29 |
| EP4036261A4 (de) | 2023-09-20 |
| CN114269957A (zh) | 2022-04-01 |
| US20220403484A1 (en) | 2022-12-22 |
| KR20220068985A (ko) | 2022-05-26 |
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