TECHNICAL FIELD
[0001] The present invention relates to a copper alloy, a copper alloy thin sheet, and a
method of manufacturing a copper alloy that are suitable as a copper alloy sheet strip
that is used, for example, in household electrical appliances, semiconductor components
such as a lead frame for a semiconductor device, electrical and electronic component
materials such as a printed wiring board, switch components, bus bars, mechanism components
such as a connector, industrial apparatuses, and the like.
BACKGROUND ART
[0003] As a copper alloy for the above-described various usages, a Cu-Fe-P-based copper
alloy that contains Fe and P is typically used in the related art. As the Cu-Fe-P-based
copper alloy, a copper alloy (CDA19400 alloy), which contains 2.1 to 2.7% by mass
of Fe, 0.015 to 0.15% by mass of P, and 0.05 to 0.20% by mass of Zn, is exemplified.
The CDA19400 alloy is an international standard alloy that is defined in Copper Development
Association (CDA).
[0004] Here, the above-described CDA19400 alloy is a precipitation strengthening type alloy
in which Fe or an intermetallic compound such as Fe-P is allowed to precipitate in
a copper parent phase, and is excellent in strength, conductivity, and thermal conductivity.
Accordingly, the CDA19400 alloy is widely used for various usages.
[0005] Recently, in accordance with usage enlargement of the Cu-Fe-P-based copper alloy,
a reduction in weight, thickness, and size of electrical or electronic apparatuses,
and the like, the CDA19400 alloy is demanded to have further higher strength or conductivity,
and excellent bending workability.
[0006] In addition, the above-described lead frame, connector, and the like are manufactured
by etching or punching the copper alloy thin sheet. Here, when punching the copper
alloy thin sheet that is composed of the CDA19400 alloy and the like, there is a problem
that abrasion in a mold is significant, and it is necessary to replace the mold after
use for a short time.
[0007] Accordingly, for example, PTL 1 and PTL 2 suggest that C is added to the Cu-Fe-P-based
alloy so as to suppress cracking in a hot-rolling process, and to improve characteristics
such as punching mold abrasion resistance. In addition, there is also suggested that
Mg and the like are added so as to improve characteristics such as strength of the
Cu-Fe-P-based alloy.
CITATION LIST
PATENT LITERATURE
DISCLOSURE OF INVENTION
TECHNICAL PROBLEM
[0009] However, in the copper alloy that is composed of the Cu-Fe-P-based alloy, when rolling
an ingot to manufacture a copper alloy thin sheet, a lot of surface defects may occur.
When the surface defects are present, a manufacturing yield ratio greatly decreases.
Therefore, there is a problem that the manufacturing cost of the copper alloy thin
sheet greatly increases.
[0010] In addition, when the copper alloy thin sheet composed of the above-described Cu-Fe-P-based
alloy is subjected to pressing, etching, or silver plating, a non-smooth shape defect
caused by coarse iron alloy particles may occur.
[0011] The invention has been made in consideration of the above-described circumstances,
and an object thereof is to provide a copper alloy, a copper alloy thin sheet, and
a method of manufacturing a copper alloy capable of suppressing occurrence of a surface
defect and a shape defect in a Cu-Fe-P-based alloy.
SOLUTION TO PROBLEM
[0012] The present inventors have conducted extensive research to solve the problem. As
a result, it was proven that surface defects and shape defects, which occur in the
Cu-Fe-P-based alloy such as the CDA19400 alloy, are formed when iron alloy particles
containing Fe and C are exposed to a surface of the copper alloy thin sheet.
[0013] In addition, it was proven that in a case where C is present in a copper alloy molten
metal in an amount that is equal to or greater than a constant amount, a liquid phase
that contains Fe as a main component and C, and a liquid phase that contains Cu as
a main component are separated from each other, and a coarse Fe-C crystallized product
is generated in the ingot. In addition, the present inventors found that the iron
alloy particles, which are exposed to the surface of the copper alloy thin sheet,
are generated due to the coarse Fe-C crystallized product generated in the ingot.
[0014] The invention has been made on the basis of the above-described finding. According
to a first aspect of the invention, there is provided a copper alloy containing 1.5
to 2.7% by mass of Fe, 0.008 to 0.15% by mass of P, and 0.01 to 0.5% by mass of Zn,
the balance being Cu and inevitable impurities. The amount of C contained as one of
the inevitable impurities is less than 3 ppm by mass.
[0015] In the copper alloy configured as described above, the amount of C contained as one
of the inevitable impurities is regulated to be less than 3 ppm by mass. As described
above, C is an element that has a function of promoting liquid phase separation between
a liquid phase that contains Fe as a main component and C, and a liquid phase that
contains Cu as a main component. Therefore, when the amount of C contained increases,
a coarse Fe-C crystallized product is likely to be generated in an ingot. Accordingly,
when regulating the amount of C contained as described above, it is possible to suppress
occurrence of the coarse Fe-C crystallized product, and it is possible to greatly
reduce surface defects due to iron alloy particles. In addition, it is possible to
suppress a shape defect of a product which is caused by the coarse Fe-C crystallized
product.
[0016] Here, the copper alloy of the invention may further contain one or both of 0.003
to 0.5% by mass of Ni and 0.003 to 0.5% by mass of Sn.
[0017] In this case, Ni or Sn is solid-soluted in a parent phase of Cu. Accordingly, it
is possible to realize an improvement in the strength of the Cu-Fe-P-based copper
alloy.
[0018] In addition, the copper alloy of the invention may further contain at least one of
Mg, Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be, Ti, and Co in a range of 0.0007
to 0.5% by mass.
[0019] In this case, it is possible to attain an improvement in the strength of the Cu-Fe-P-based
alloy and an improvement in punching mold abrasion resistance due to an element such
as Mg, Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be, Ti, and Co.
[0020] In addition, in the copper alloy of the invention, the amount of Mn contained as
one of the inevitable impurities may be 20 ppm by mass or less, and the amount of
Ta contained as one of the inevitable impurities may be 1 ppm by mass or less.
[0021] When the liquid phase separation occurs in the copper alloy molten metal as described
above, an element such as Mn and Ta is contained in the liquid phase that contains
Fe as a main component and C, and tends to promote the liquid phase separation. Therefore,
there is a concern that when Mn and Ta, which are inevitable impurities, are contained
in a large amount, the coarse Fe-C crystallized product is likely to be generated
in an ingot. Therefore, when the amount of Mn contained is regulated to 20 ppm by
mass or less, and the amount of Ta contained is regulated to 1 ppm by mass or less,
it is possible to reliably suppress occurrence of the coarse Fe-C crystallized product.
[0022] According to a second aspect of the invention, there is provided a copper alloy thin
sheet that is composed of the above-described copper alloy. The number of surface
defects, which have a length of 200 µm or greater and are formed when iron alloy particles
containing Fe and C are exposed to a surface, are 5 pieces/m
2 or less. More preferably, the number of the surface defects having a length of 200
µm or greater is 2 pieces/m
2 or less, and still more preferably less than 1 piece/m
2.
[0023] In addition, in the copper alloy thin sheet of the invention, the thickness of the
thin sheet may be 0.5 mm or less.
[0024] According to the copper alloy thin sheet configured as described above, the copper
alloy thin sheet is composed of a copper alloy in which the amount of C contained
as one of the inevitable impurities is suppressed to be low. Accordingly, occurrence
of iron alloy particles containing Fe and C is suppressed, and it is possible to suppress
occurrence of the surface defects which are caused by the iron alloy particles. In
addition, it is possible to suppress the shape defect of a product which is caused
by the coarse Fe-C crystallized product. In addition, when the number of the surface
defects having a length of 200 µm or greater is 5 pieces/m
2 or less, it is possible to significantly decrease a product failure rate when performing
pressing, etching, or silver plating. Particularly, when the sheet thickness of the
copper alloy thin sheet is 0.5 mm or less and surface defects of 200 µm or greater
exist, there is a concern that defects also exist in a thickness direction. Therefore,
for example, when machining a precise shape such as pressing and etching, the surface
defects may cause a failure. From the above-described viewpoint, when the sheet thickness
of the copper alloy thin sheet is 0.2 mm or less, the effect of the invention is further
exhibited. When considering the manufacturing cost of the copper alloy thin sheet
and the effect that is obtained, it is preferable that the lower limit of the sheet
thickness of the thin sheet be set to 0.05 mm, but there is no limitation thereto.
[0025] According to a third aspect of the invention, a method is provided for manufacturing
a copper alloy. The method includes a melting process of melting a raw material to
produce a copper alloy molten metal, a high-temperature holding process of holding
the copper alloy molten metal at 1300°C or higher, and a casting process of supplying
the copper alloy molten metal, which is held at 1300°C or higher, into a mold so as
to obtain an ingot.
[0026] As described above, the method of manufacturing a copper alloy includes the high-temperature
holding process of holding the copper alloy molten metal at 1300°C or higher, and
the casting process of supplying the copper alloy molten metal, which is held at a
temperature as high as 1300°C or higher, into a mold so as to obtain an ingot. Accordingly,
in the copper alloy molten metal, it is possible to suppress the liquid phase separation
between the liquid phase that contains Fe as a main component and C, and the liquid
phase that contains Cu as a main component, and it is possible to suppress generation
of the coarse Fe-C crystallized product. Accordingly, it is possible to reduce the
surface defects which are caused by the iron alloy particles. In addition, it is possible
to suppress the shape defect of the product which is caused by the coarse Fe-C crystallized
product.
ADVANTAGEOUS EFFECTS OF INVENTION
[0027] According to the invention, it is possible to provide a copper alloy, a copper alloy
thin sheet, and a method of manufacturing a copper alloy capable of suppressing occurrence
of a surface defect and a shape defect in a Cu-Fe-P-based alloy.
BRIEF DESCRIPTION OF DRAWINGS
[0028]
FIG. 1 is a photograph obtained by observing a surface defect of a copper alloy thin
sheet with an optical microscope.
FIG. 2 is a flowchart illustrating a method of manufacturing a copper alloy according
to an embodiment of the invention.
BEST MODE FOR CARRYING-OUT THE INVENTION
[0029] Hereinafter, description will be given of a copper alloy according to a first embodiment
of the invention.
[0030] The copper alloy according to the first embodiment of the invention contains 1.5
to 2.7% by mass of Fe, 0.008 to 0.15% by mass of P, and 0.01 to 0.5% by mass of Zn,
the balance being Cu and inevitable impurities. The amount of C contained as one of
the inevitable impurities is less than 3 ppm by mass.
[0031] Hereinafter, description will be given of the reason why the amounts of the elements
contained are set in the above-described ranges.
[Fe]
[0032] Fe is solid-soluted in a parent phase of Cu, and generates P-containing precipitates
(Fe-P compounds). When the Fe-P compounds are dispersed in the parent phase of Cu,
strength and hardness are improved without decreasing conductivity.
[0033] Here, when the amount of Fe contained is less than 1.5% by mass, the effect of improving
the strength, and the like are not sufficient. On the other hand, when the amount
of Fe contained exceeds 2.7% by mass, a large crystallized product is generated. Therefore,
there is a concern that surface cleanliness may be deteriorated. In addition, there
is a concern that a decrease in conductivity and workability may be caused.
[0034] Accordingly, in this embodiment, the amount of Fe contained is 1.5 to 2.7% by mass.
It is preferable that the amount of Fe contained be set in a range of 1.8 to 2.6%
by mass so as to reliably exhibit the above-described operation effect.
[P]
[0035] P is an element having a deoxidizing operation. In addition, as described above,
P generates Fe-P compounds in combination with Fe. When the Fe-P compounds are dispersed
in the parent phase of Cu, the strength and the hardness are improved without decreasing
the conductivity.
[0036] Here, when the amount of P contained is less than 0.008% by mass, the effect of improving
the strength, and the like are not sufficient. On the other hand, when the amount
of P contained exceeds 0.15% by mass, a decrease in the conductivity and the workability
is caused.
[0037] Accordingly, in this embodiment, the amount of P contained is 0.008 to 0.15% by mass.
It is preferable that the amount of P contained be set in a range of 0.01 to 0.05%
by mass so as to reliably exhibit the above-described operation effect.
[Zn]
[0038] Zn is an element that is solid-soluted in the parent phase of Cu and has an operation
of improving solder thermal-peeling resistance.
[0039] Here, when the amount of Zn contained is less than 0.01% by mass, the operation effect
of improving the solder thermal-peeling resistance cannot be sufficiently exhibited.
On the other, even when the amount of Zn contained exceeds 0.5% by mass, the above-described
effect is saturated.
[0040] Accordingly, in this embodiment, the amount of Zn contained is 0.01 to 0.5% by mass.
It is preferable that the amount of Zn contained be set in a range of 0.05 to 0.35%
by mass so as to reliably exhibit the above-described operation effect.
[C]
[0041] C is contained in the above-described copper alloy as an inevitable impurity. Here,
in a case where a large amount of C is contained, a surface defect of a copper alloy
thin sheet greatly increases. A result obtained by observing an example of the surface
defect with an optical microscope is illustrated in FIG. 1.
[0042] From an analysis result with an electron probe micro analyzer (EPMA), the surface
defect that is observed in this embodiment is caused by iron alloy particles containing
Fe and C.
[0043] Typically, when melting and casting the above-described copper alloy, the Fe element
is present in a state of being melted in a liquid phase that contains Cu as a main
component. However, when C is present in an amount that is equal to or greater than
a constant amount, in a copper alloy molten metal, the liquid phase that contains
Cu as a main component, and a liquid phase that contains Fe as a main component and
C are separated from each other. As a result, a coarse Fe-C crystallized product is
present in an ingot. Then, when the ingot is rolled, it is considered that iron alloy
particles, which are caused by the coarse Fe-C crystallized product, are exposed to
a surface of the copper alloy thin sheet, and the above-described surface defect occurs.
In addition, when performing pressing, etching, or silver plating, a shape defect
occurs due to the iron alloy particles.
[0044] Accordingly, when the element C is reduced, it is possible to suppress the surface
defect and the shape defect which are caused by the iron alloy particles. Accordingly,
in this embodiment, the amount of C contained is limited to be less than 3 ppm by
mass. It is preferable that the amount of C contained be set to be less than 2 ppm
by mass so as to reliably accomplish suppression of the surface defect and the shape
defect.
[0045] Examples of the inevitable impurities other than C include Ni, Sn, Mg, Ca, Sr, Ba,
rare-earth elements, Zr, Si, Al, Be, Ti, H, Li, B, N, O, F, Na, S, Cl, K, V, Cr, Mn,
Co, Ga, Ge, As, Se, Br, Rb, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sb, Te, I, Cs, Hf,
Ta, W, Re, Os, Ir, Pt, Au, Hg, Tl, Pb, Bi, and the like. It is preferable that these
inevitable impurities be contained in a total amount of 0.3% by mass or less. When
considering the manufacturing cost of the copper alloy and an effect that is obtained,
the lower limit of the total amount of the inevitable impurities is preferably 0.1%
by mass, but there is no limitation thereto.
[0046] Next, description will be given of an example of the method of manufacturing the
copper alloy according to this embodiment with reference to a flowchart illustrated
in FIG. 2.
[Melting Process S01]
[0047] A copper alloy molten metal is generated by melting a copper raw material, pure iron,
Zn or a Cu-Zn parent alloy, and P or a Cu-P parent alloy. In addition, as the copper
raw material, so-called 4N Cu having purity of 99.99% by mass or greater is preferable.
As the pure iron, so-called 3N Fe having purity of 99.9% by mass or greater or so-called
4N Fe having purity of 99.99% by mass or greater is preferable. As an atmosphere,
Ar is preferable. A melting temperature is set to, for example, 1100 to 1300°C.
[High-temperature holding process S02]
[0048] Next, a temperature of the copper alloy molten metal that is obtained is raised to
1300°C or higher and is held at the temperature. When the copper alloy molten metal
is held at the high temperature, it is possible to suppress the liquid phase separation
in the copper alloy molten metal. In the high-temperature holding process S02, it
is preferable that the temperature be set in a range of 1300 to 1500°C, and holding
time is set in a range of 1 minute to 24 hours.
[Casting Process S03]
[0049] In addition, the copper alloy molten metal that is held at a temperature of 1300°C
or higher is poured into a mold in a state of being held at the high temperature,
thereby producing an ingot. According to this, the ingot of the copper alloy according
to this embodiment is produced.
[0050] Here, it is preferable that a cooling rate during casting be as fast as possible.
For example, it is preferable that the cooling rate from 1300 to 900°C be 5 °C/s or
greater, more preferably 10 °C/s or greater. When considering the manufacturing cost
of the copper alloy and the effect that is obtained, it is preferable that the upper
limit of the cooling rate be 200 °C/s, but there is no limitation thereto.
[0051] After subjecting the ingot that is obtained to hot-rolling, cold-rolling and a heat
treatment are appropriately repeated to produce a copper alloy thin sheet having a
predetermined thickness. Hot-rolling is performed in a reducing atmosphere under a
condition of 750 to 1000°C. Cold-rolling reduction is set to 40 to 95%, heat treatment
is performed at 400 to 700°C, and final annealing is performed at 200 to 350°C after
final rolling.
[0052] In the copper alloy thin sheet, the number of surface defects, which have a length
of 200 µm or greater and are formed when the iron alloy particles containing Fe and
C are exposed to a surface, is 5 pieces/m
2 or less. Preferably, the number of surface defects having a length of 200 µm or greater
is 2 pieces/m
2 or less, and more preferably 1 piece/m
2 or less.
[0053] According to this embodiment configured as described above, since the amount of C,
which is one of the inevitable impurities, is less than 3 ppm by mass, it is possible
to suppress generation of the coarse Fe-C crystallized product in the ingot. Accordingly,
it is possible to suppress formation of the iron alloy particles which are caused
by the coarse Fe-C crystallized product, and it is possible to greatly reduce occurrence
of the surface defect. In addition, it is possible to suppress a shape defect of a
product.
[0054] In addition, since the manufacturing method according to this embodiment includes
the high-temperature holding process S02 of holding the copper alloy molten metal
at a high temperature of 1300°C or higher, and the casting process S03 of supplying
the copper alloy molten metal, which is held at 1300°C or higher, into a mold to manufacture
the ingot, it is possible to suppress generation of the coarse Fe-C crystallized product.
[0055] Hereinafter, description will be given of a copper alloy according to a second embodiment
of the invention.
[0056] The copper alloy according to the second embodiment of the invention contains 1.5
to 2.7% by mass of Fe, 0.008 to 0.15% by mass of P, 0.01 to 0.5% by mass of Zn, any
one or both of 0.003 to 0.5% by mass of Ni and 0.003 to 0.5% by mass of Sn, and at
least one or more of Mg, Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be, Ti, and
Co in a range of 0.0007 to 0.5% by mass, the balance being Cu and inevitable impurities.
The amount of C contained as one of the inevitable impurities is less than 3 ppm by
mass.
[0057] Hereinafter, description will be given of the reason why the amounts of the elements
contained are set in the above-described ranges. In addition, description of the same
elements as in the first embodiment will not be repeated.
[Ni]
[0058] Ni is solid-soluted in the parent phase of Cu, and has an operation of improving
the strength and lead bending fatigue resistant characteristics (repetitive bending
fatigue resistant characteristics).
[0059] Here, when the amount of Ni contained is less than 0.003% by mass, it is difficult
to sufficiently exhibit the above-described effects. On the other hand, when the amount
of Ni contained exceeds 0.5% by mass, the conductivity significantly decreases.
[0060] Accordingly, in this embodiment, the amount of Ni contained is 0.003 to 0.5% by mass.
It is preferable that the amount of Ni contained be set in a range of 0.008 to 0.2%
by mass so as to reliably exhibit the above-described operation effect.
[Sn]
[0061] Sn is solid-soluted in the parent phase of Cu, and has an operation of improving
the strength and solderability.
[0062] Here, when the amount of Sn contained is less than 0.003% by mass, it is difficult
to sufficiently exhibit the above-described effect. On the other hand, when the amount
of Sn contained exceeds 0.5% by mass, the conductivity significantly decreases.
[0063] Accordingly, in this embodiment, the amount of Sn contained is 0.003 to 0.5% by mass.
It is preferable that the amount of Sn contained be set in a range of 0.008 to 0.2%
by mass so as to reliably exhibit the above-described operation effect.
[Mg, Ca, Sr, Ba, Rare-Earth Elements, Zr, Si, Al, Be, Ti, and Co]
[0064] Mg, Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be, Ti, and Co are solid-soluted
in the parent phase of Copper, or are present as a precipitate or a crystallized product,
and have an operation of improving the strength of the Cu-Fe-P-based alloy and an
operation of improving punching mold abrasion resistance.
[0065] Here, when the amount of Mg, Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be, Ti,
and Co, which are contained, is less than 0.0007% by mass, it is difficult to exhibit
the above-described effect. On the other hand, when the amount of Mg, Ca, Sr, Ba,
the rare-earth elements, Zr, Si, Al, Be, Ti, and Co, which are contained, exceeds
0.5% by mass, the conductivity greatly decreases, and a large oxide, precipitate,
or crystallized product is likely to be generated, and there is a concern that the
surface cleanliness may be deteriorated.
[0066] Accordingly, in the copper alloy of this embodiment, the amount of Mg, Ca, Sr, Ba,
the rare-earth elements, Zr, Si, Al, Be, Ti, and Co, which are contained, is 0.0007
to 0.5% by mass. In addition, it is preferable that the amount of Mg, Ca, Sr, Ba,
the rare-earth elements, Zr, Si, Al, Be, Ti, and Co, which are contained, be set in
a range of 0.005 to 0.15% by mass so as to reliably exhibit the above-described operation
effect.
[0067] Here, the rare-earth elements represent Sc, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy,
Ho, Er, Tm, Yb, and Lu.
[0068] Examples of the inevitable impurities other than C include H, Li, B, N, O, F, Na,
S, Cl, K, V, Cr, Mn, Ga, Ge, As, Se, Br, Rb, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sb,
Te, I, Cs, Hf, Ta, W, Re, Os, Ir, Pt, Au, Hg, Tl, Pb, Bi, and the like. It is preferable
that the total amount of the inevitable impurities be 0.3% by mass or less. When considering
the manufacturing cost of the copper alloy and the effect that is obtained, it is
preferable that the lower limit of the total amount of the inevitable impurities be
set to 0.1% by mass, but there is no limitation thereto.
[0069] As is the case with the first embodiment, the copper alloy according to the second
embodiment is manufactured by the melting process S01, the high-temperature holding
process S02 of the molten metal, and the casting process S03. In the melting process
S01, for addition ofNi, Sn, Mg, Ca, Sr, Ba, the rare-earth elements, Zr, Si, Al, Be,
Ti, and Co, metal element elementary substances or parent alloys containing the elements
are used.
[0070] According to this embodiment configured as described above, since Ni and Sn are
contained, it is possible to realize an improvement of the strength through solid-solution
strengthening.
[0071] In addition, since at least one of Mg, Ca, Sr, Ba, the rare-earth elements, Zr, Si,
Al, Be, Ti, and Co are contained in a range of 0.0007 to 0.5% by mass, it is possible
to realize additional high strengthening of the Cu-Fe-P-based alloy, and it is possible
to realize an improvement of the punching mold abrasion resistance.
[0072] In addition, since the amount of C contained is less than 3 ppm by mass, it is possible
to suppress formation of the iron alloy particles containing Fe and C, and it is possible
to greatly reduce occurrence of the surface defect. In addition, it is possible to
suppress the shape defect in a product.
[0073] Hereinafter, description will be given of a copper alloy according to a third embodiment
of the invention.
[0074] The copper alloy according to the third embodiment of the invention contains 1.5
to 2.7% by mass of Fe, 0.008 to 0.15% by mass of P, and 0.01 to 0.5% by mass of Zn,
the balance being Cu and inevitable impurities. The amount of C contained as one of
the inevitable impurities is less than 3 ppm by mass, the amount of Mn contained as
one of the inevitable impurities is 20 ppm by mass or less, and the amount of Ta contained
as one of the inevitable impurities is 1 ppm by mass or less.
[0075] Hereinafter, description will be given of the reason why the amounts of the elements
contained are set in the above-described ranges. In addition, description of the same
elements as in the first embodiment will not be repeated.
[Mn and Ta]
[0076] Mn and Ta are inevitable impurities, and are contained in the above-described copper
alloy.
[0077] Typically, when melting and casting the above-described copper alloy, the Fe element
is present in a state of being melted in a liquid phase that contains Cu as a main
component. However, in a case where C is present in an amount that is equal to or
greater than a constant amount, in the copper alloy molten metal, the liquid phase
that contains Cu as a main component, and a liquid phase that contains Fe as a main
component and C are separated from each other. Here, when the liquid phase separation
occurs in the copper alloy molten metal as described above, Mn and Ta are elements
which are contained in the liquid phase that contains Fe as a main component and C,
and may promote the liquid phase separation.
[0078] Accordingly, when the element C is reduced, and the amount of Mn and Ta, which are
contained, is reduced, it is possible to suppress the liquid phase separation in the
copper alloy molten metal. As a result, it is possible to suppress generation of the
coarse Fe-C crystallized product, and it is possible to suppress the surface defect
and the shape defect which are caused by the iron alloy particles. Accordingly, in
the copper alloy according to this embodiment, the amount of C contained is limited
to be less than 3 ppm by mass, the amount of Mn contained is limited to 20 ppm by
mass or less, and the amount of Ta contained is limited to 1 ppm by mass or less.
It is preferable that the amount of C contained be set to be less than 2 ppm by mass,
the amount of Mn contained is less than 15 ppm by mass, and the amount of Ta contained
is less than 0.7 ppm by mass so as to reliably accomplish suppression of the surface
defect and the shape defect.
[0079] Examples of the inevitable impurities other than C, Mn, and Ta include Ni, Sn, Mg,
Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be, Ti, H, Li, B, N, O, F, Na, S, Cl,
K, V, Cr, Co, Ga, Ge, As, Se, Br, Rb, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sb, Te,
I, Cs, Hf, W, Re, Os, Ir, Pt, Au, Hg, Tl, Pb, Bi, and the like. It is preferable that
the total amount of the inevitable impurities be 0.3% by mass or less. When considering
the manufacturing cost of the copper alloy and the effect that is obtained, the lower
limit of the total amount of the inevitable impurities is preferably 0.1% by mass,
but there is no limitation thereto.
[0080] As is the case with the first embodiment and the second embodiment, the copper alloy
according to the third embodiment is manufactured by the melting process S01, the
high-temperature holding process S02 of the molten metal, and the casting process
S03.
[0081] In the melting process S01, it is preferable to use a raw material in which the amount
of Mn and Ta contained is small. Particularly, there is a high possibility that the
element Mn is mixed-in from an iron-based raw material and the like. Accordingly,
it is preferable that the iron-based raw material be carefully selected and used.
Preferably, an Fe raw material, which contains 0.1% by mass or less of Mn and 0.005%
by mass or less of Ta, is used.
[0082] According to this embodiment configured as described above, since the amount of C
contained as one of the inevitable impurities is less than 3 ppm by mass, the amount
of Mn contained as one of the inevitable impurities is 20 ppm or less, and the amount
of Ta contained as one of the inevitable impurities is 1 ppm by mass or less, it is
possible to suppress the liquid phase separation in the copper alloy molten metal
and the formation of the iron alloy particles containing Fe and C. As a result, it
is possible to greatly reduce occurrence of the surface defect. In addition, it is
possible to suppress the shape defect of a product.
[0083] Hereinbefore, description has given of the copper alloy, the copper alloy thin sheet,
and the method of manufacturing a copper alloy according to the embodiments of the
invention. However, the invention is not limited thereto and can be appropriately
modified in a range not departing from the technical spirit of the invention.
[0084] For example, description has been given of a configuration in which the copper raw
material is melted to produce the copper molten metal, and various elements are added
to the copper molten metal. However, there is no limitation thereto, and component
preparation may be performed by melting a scrap raw material and the like.
[0085] In addition, in this embodiment, description has been given of a configuration in
which the high-temperature holding process S02 is provided. However, there is no limitation
thereto, and the amount of C contained may be reduced by another means. For example,
the element C may be prevented from being mixed-in through careful selection of a
raw material that is used. There is a high possibility that the element C may be mixed-in
from an iron-based raw material and the like. Accordingly, it is preferable that the
iron-based raw material be carefully selected and used.
[0086] In addition, in the third embodiment, any one or both of 0.003 to 0.5% by mass of
Ni and 0.003 to 0.5% by mass of Sn may be contained, and at least of Mg, Ca, Sr, Ba,
rare-earth elements, Zr, Si, Al, Be, Ti, and Co may be contained in a range of 0.0007
to 0.5% by mass.
EXAMPLES
[0087] Hereinafter, description will be given of results of a confirmation experiment that
was performed to confirm the effect of the invention.
(Example 1)
[0088] A copper raw material composed of oxygen-free copper (ASTM B152 C10100), which had
purity of 99.99% by mass or greater and in which the amount of C contained was 1 ppm
by mass or less, was prepared. The copper raw material was placed in an alumina crucible,
and was melted by using a high-frequency melting furnace that was set to an Ar gas
atmosphere.
[0089] As raw materials, pure iron, a Cu-Zn parent alloy, a Cu-Ni parent alloy, a Cu-Sn
parent alloy, a Cu-P parent alloy, and raw materials or parent alloys of Mg, Ca, Sr,
Ba, rare-earth elements, Zr, Si, Al, Be, Ti, and Co were added to the resultant copper
molten metal, which was obtained, according to the necessity, and then melting was
performed at 1200°C in an Ar atmosphere for preparation in a component composition
illustrated in Table 1. Then, the resultant molten metal that was prepared was poured
into a water-cooled copper mold to produce an ingot. In addition, the amount of C
contained in each raw material was 10 ppm by mass or less. The size of the ingot that
was produced was set to have a thickness of approximately 30 mm, a width of approximately
150 mm, and a length of approximately 200 mm. In addition, in Examples 1 to 27, as
the iron raw material, high-purity iron (purity of 99.99% by mass) was used.
[0090] In addition, in Examples 23 to 26, a temperature of the molten metal, which was obtained,
was raised once from 1200 to 1300°C, and then the ingot was produced.
[0091] A cooling rate from 1300 to 900°C when the temperature of the molten metal was set
to 1300°C, and a cooling rate from 1200 to 900°C when the temperature of the molten
metal was set to 1200°C were set to approximately 10 °C/s or greater.
[0092] In addition, in Comparative Examples 1 and 2, a C powder was added to the molten
metal to come into contact therewith, thereby increasing the amount of C.
[0093] The ingot, which was obtained, was heated at 950°C, and hot-rolling was performed
up to a thickness of 5.0 mm. After the hot-rolling, surface grinding was performed
to remove an oxidized film, and the thickness was set to 4.0 mm.
[0094] Then, rough rolling was performed to set the thickness to 0.4 mm. Next, a heating
process was performed at 550°C for 1 hour, and then cold-rolling was additionally
performed to set the thickness to 0.2 mm.
[0095] Next, a heating process was performed at 450°C for 1 hour, and final cold-rolling
was performed to produce a strip material having a thickness of approximately 0.1
mm and a width of approximately 150 mm.
[0096] In addition, a heating process was performed at 250°C for 1 hour as final annealing,
and a strip material, which was obtained, was set as a strip material for evaluation
of characteristics. Here, all of the heat treatments were performed in an Ar atmosphere.
[0097] The following characteristic evaluation was performed by using the obtained strip
material for evaluation of characteristics.
(Method of Measuring Amount of Fe, P, Zn, Other Additional Elements, and Impurity)
[0098] In compositions of Table 1, Fe, P, Zn, and other additional elements were measured
with a glow discharge mass spectrometer (GD-MS), and C was measured with an infrared
absorption spectrometry.
(Mechanical Characteristics)
[0099] A test specimen of No. 13B, which is defined in JIS Z 2241: 2011 (based on ISO 6892-1:
2009), was collected from the strip material for evaluation of characteristics, and
0.2% proof stress was measured in accordance with an offset method.
[0100] In addition, the test specimen was collected in such a manner that a tensile direction
during a tensile test becomes parallel to a rolling direction of the strip material
for evaluation of characteristics.
(Number of Defects)
[0101] With respect to 25 sheets of copper strips which were obtained from the strip material
for evaluation of characteristics and had the size of 0.2 m
2, the number of surface defects, which had a length of 200 µm or greater and were
formed when foreign substances were exposed to a surface, was inspected. The length
of the defects was set to the maximum length of a surface damage, which occurred when
the foreign substances were exposed to the surface, in the rolling direction. In accordance
with the evaluation method, an average number of defects (pieces/m
2) was calculated.
[0102] Evaluation results are illustrated in Table 1.
[Table 1]
| |
Component composition |
Impurity |
High-temperature holding process |
Average number of defects (pieces/m2) |
0.2% proof stress (MPa) |
| Fe (% by mass) |
P (% by mass) |
Zn (% by mass) |
Others (% by mass) |
Cu |
C (ppm by mass) |
| |
1 |
1.6 |
0.027 |
0.076 |
- |
- |
Balance |
0.8 |
Not performed |
0.2 |
480 |
| |
2 |
2.5 |
0.025 |
0.072 |
- |
- |
Balance |
2.4 |
Not performed |
1.8 |
481 |
| |
3 |
2.2 |
0.011 |
0.074 |
- |
- |
Balance |
2.0 |
Not performed |
0.4 |
485 |
| |
4 |
2.1 |
0.146 |
0.073 |
- |
- |
Balance |
2.0 |
Not performed |
0.4 |
484 |
| |
5 |
2.3 |
0.025 |
0.021 |
- |
- |
Balance |
1.7 |
Not performed |
0.2 |
484 |
| |
6 |
2.1 |
0.025 |
0.396 |
- |
- |
Balance |
2.1 |
Not performed |
0.4 |
483 |
| |
7 |
2.2 |
0.028 |
0.074 |
- |
- |
Balance |
2.1 |
Not performed |
0.4 |
483 |
| |
8 |
2.2 |
0.029 |
0.067 |
Ni |
0.034 |
Balance |
2.1 |
Not performed |
0.4 |
508 |
| |
9 |
2.2 |
0.028 |
0.071 |
Sn |
0.081 |
Balance |
1.7 |
Not performed |
0.2 |
509 |
| |
10 |
2.1 |
0.026 |
0.067 |
Mg |
0.015 |
Balance |
1.9 |
Not performed |
0.2 |
509 |
| |
11 |
2.2 |
0.026 |
0.067 |
Ca |
0.010 |
Balance |
2.2 |
Not performed |
0.4 |
498 |
| |
12 |
2.1 |
0.025 |
0.076 |
Sr |
0.008 |
Balance |
2.0 |
Not performed |
0.4 |
498 |
| |
13 |
2.2 |
0.029 |
0.070 |
Ba |
0.009 |
Balance |
2.0 |
Not performed |
0.4 |
499 |
| |
14 |
2.2 |
0.029 |
0.076 |
La |
0.009 |
Balance |
1.9 |
Not performed |
0.2 |
500 |
| |
15 |
2.2 |
0.028 |
0.071 |
Zr |
0.006 |
Balance |
1.9 |
Not performed |
0.2 |
506 |
| |
16 |
2.3 |
0.029 |
0.066 |
Si |
0.015 |
Balance |
1.6 |
Not performed |
0.2 |
502 |
| Examples |
17 |
2.3 |
0.029 |
0.067 |
Al |
0.032 |
Balance |
2.1 |
Not performed |
0.4 |
506 |
| |
18 |
2.1 |
0.025 |
0.071 |
Be |
0.009 |
Balance |
1.7 |
Not performed |
0.2 |
505 |
| |
19 |
2.1 |
0.028 |
0.074 |
Ti |
0.010 |
Balance |
2.0 |
Not performed |
0.2 |
506 |
| |
20 |
2.2 |
0.027 |
0.069 |
Ni |
0.027 |
Balance |
2.0 |
Not performed |
0.2 |
505 |
| |
Co |
0.032 |
| |
21 |
2.2 |
0.029 |
0.064 |
Sn |
0.023 |
Balance |
2.1 |
Not performed |
0.4 |
505 |
| |
Co |
0.014 |
| |
22 |
2.1 |
0.025 |
0.066 |
Ni |
0.024 |
Balance |
1.7 |
Not performed |
0.2 |
507 |
| |
Sn |
0.006 |
| |
Si |
0.015 |
| |
Al |
0.016 |
| |
23 |
2.1 |
0.026 |
0.071 |
- |
- |
Balance |
1.8 |
Performed |
0.2 |
479 |
| |
24 |
2.2 |
0.025 |
0.077 |
Ni |
0.028 |
Balance |
1.8 |
Performed |
0.2 |
497 |
| |
25 |
2.3 |
0.027 |
0.076 |
Sn |
0.027 |
Balance |
1.7 |
Performed |
0.2 |
508 |
| |
26 |
2.1 |
0.029 |
0.075 |
Ni |
0.032 |
Balance |
1.7 |
Performed |
0.2 |
507 |
| |
Si |
0.014 |
| |
27 |
2.7 |
0.026 |
0.066 |
- |
- |
Balance |
2.9 |
Not performed |
4.4 |
485 |
| Comparative Examples |
1 |
2.3 |
0.029 |
0.072 |
- |
- |
Balance |
14.3 |
Not performed |
11.2 |
483 |
| 2 |
2.4 |
0.026 |
0.076 |
Ni |
0.031 |
Balance |
13.0 |
Not performed |
11.0 |
512 |
| Si |
0.011 |
[0103] In Comparative Examples 1 and 2 in which the amount of C contained as one of the
inevitable impurities exceeded the range of the invention, the number of defects was
as large as 11.2 pieces/m
2 and 11.0 pieces/m
2, respectively.
[0104] In contrast, in Examples 1 to 27 in which the amount of C as the inevitable impurity
was less than 3 ppm by mass, the number of defects was 4.4 pieces/m
2 or less, and it was confirmed that the number of defects was greatly reduced in comparison
to Comparative Examples.
[0105] In Examples 8 to 22, and 24 to 26 in which Mg, Ca, Sr, Ba, the rare-earth elements,
Zr, Si, Al, Be, Ti, and Co were added, the 0.2% proof stress was approximately 500
MPa, and an improvement in the strength characteristics was confirmed.
[0106] In Examples 23 to 26 in which the ingot was produced after the copper alloy molten
metal was held at 1300°C, and high-temperature holding of the molten metal was performed,
the number of defects was further reduced. From this result, it was confirmed that
it is possible to further suppress the surface defects of the copper alloy thin sheet
by performing the high-temperature holding of the copper alloy molten metal.
(Example 2)
[0107] A copper raw material composed of oxygen-free copper (ASTM B152 C10100), which had
purity of 99.99% by mass or greater and in which the amount of C contained was 1 ppm
by mass or less, the amount of Mn contained was 0.1 ppm by mass or less, and the amount
of Ta contained was 0.1 ppm by mass or less, was prepared. The copper raw material
was placed in an alumina crucible, and was melted by using a high-frequency melting
furnace that was set to an Ar gas atmosphere.
[0108] As raw materials, pure iron, an Fe-Mn parent alloy, an Fe-Ta parent alloy, a Cu-Zn
parent alloy, a Cu-Ni parent alloy, a Cu-Sn parent alloy, a Cu-P parent alloy, raw
materials or parent alloys of Mg, Ca, Sr, Ba, rare-earth elements, Zr, Si, Al, Be,
Ti, and Co were added to the resultant copper molten metal, which was obtained, according
to the necessity, and an ingot (thickness of approximately 30 mm x width of approximately
150 mm x length of approximately 200 mm) having a component composition illustrated
in Table 2 was produced by the same method as in Example 1. In Examples 39 to 41,
a temperature of the molten metal, which was obtained, was raised once from 1200 to
1300°C, and then the ingot was produced.
[0109] A strip material for evaluation of characteristics having a thickness of approximately
0.1 mm and a width of approximately 150 mm was produced by the same method as in Example
1 by using the ingot.
[0110] The following characteristic evaluation was performed by using the obtained strip
material for evaluation of characteristics.
[0111] With regard to the number of defects, both front and rear surfaces of 50 sheets of
copper strips of 0.2 m
2, which were obtained from the strip material for evaluation of characteristics, were
observed for more detailed evaluation, and the number of surface defects, which had
a length of 200 µm or greater and were formed when foreign substances were exposed
to a surface, was inspected. The length of the defects was set to the maximum length
of a surface damage, which occurred when the foreign substances were exposed to the
surface, in the rolling direction. In accordance with the evaluation method, an average
number of defects (pieces/m
2) was calculated.
(Method of Measuring Amount of Fe, P, Zn, Mn, Ta, Other Additional Elements, and Impurity)
[0112] Fe, P, and Zn were measured with an inductively coupled plasma atomic emission spectrometer
(ICP-AES). Mn, Ta, and other additional elements were measured with the glow discharge
mass spectrometer (GD-MS).
[0113] C was measured with the infrared absorption spectrometry.
[0114] Evaluation results are illustrated in Table 2.
[Table 2]
| |
Component composition (% by mass) |
Impurities (ppm by mass) |
High-temperature holding process |
Average number of defects (pieces/m2) |
| Fe |
P |
Zn |
Others |
Cu |
C |
Mn |
Ta |
| |
31 |
2.3 |
0.029 |
0.074 |
- |
- |
Balance |
1.7 |
25.0 |
1.7 |
Not performed |
0.50 |
| |
32 |
2.2 |
0.030 |
0.064 |
- |
- |
Balance |
2.6 |
32.0 |
2.5 |
Not performed |
0.85 |
| |
33 |
2.1 |
0.025 |
0.077 |
Ni |
0.035 |
Balance |
1.3 |
27.0 |
1.3 |
Not performed |
0.35 |
| |
34 |
2.2 |
0.025 |
0.067 |
Mg |
0.023 |
Balance |
0.8 |
22.0 |
2.8 |
Not performed |
0.20 |
| |
35 |
2.3 |
0.028 |
0.076 |
- |
- |
Balance |
1.6 |
14.0 |
0.9 |
Not performed |
0.15 |
| Examples |
36 |
2.1 |
0.027 |
0.077 |
- |
- |
Balance |
2.5 |
7.0 |
0.1 |
Not performed |
0.15 |
| |
37 |
2.2 |
0.027 |
0.070 |
Ni |
0.034 |
Balance |
1.7 |
15.0 |
0.7 |
Not performed |
0.10 |
| |
38 |
2.2 |
0.025 |
0.071 |
Mg |
0.021 |
Balance |
1.8 |
14.0 |
0.1 |
Not performed |
0.05 |
| |
39 |
2.2 |
0.025 |
0.075 |
- |
- |
Balance |
1.4 |
4.0 |
0.1 |
Performed |
0.05 |
| |
40 |
2.3 |
0.026 |
0.076 |
Ni |
0.032 |
Balance |
1.6 |
18.0 |
0.2 |
Performed |
0.10 |
| |
41 |
2.3 |
0.024 |
0.066 |
Mg |
0.030 |
Balance |
1.8 |
10.0 |
0.1 |
Performed |
0.10 |
[0115] In Examples 35 to 41 in which the amount of Mn contained as one of the inevitable
impurities was defined to 20 ppm by mass or less, and the amount of Ta contained as
one of the inevitable impurities was defined to 1 ppm by mass or less, the average
number of defects was further reduced.
[0116] From this result, it was confirmed that it is possible to further suppress the surface
defects of the copper alloy thin sheet by setting the amount of Mn contained as one
of the inevitable impurities to 20 ppm by mass or less, and the amount of Ta contained
as one of the inevitable impurities to 1 ppm by mass or less.
INDUSTRIAL APPLICABILITY
[0117] According to the copper alloy, the copper alloy thin sheet, and the method of manufacturing
a copper alloy according to the invention, it is possible to suppress occurrence of
the surface defects and the shape defect in the Cu-Fe-P-based alloy.
REFERENCE SIGNS LIST
[0118]
- S01:
- Melting process
- S02:
- High-temperature holding process
- S03:
- Casting process
- RD:
- Rolling direction
- L:
- Length of surface defect