TECHNICAL FIELD
[0001] The present invention relates to a copper alloy of a Cu-Ni-Si system for an electrical
and electronic device, and to a method for producing the same. The copper alloy is
suitable for a lead frame, a connector, a terminal, a relay, a switch, or the like
of an electrical and electronic device.
BACKGROUND ART
[0002] Conventionally, there has been widely used a copper-based material with superior
electrical and thermal conductivity such as phosphor bronze, red brass, brass, a Corson
alloy, or the like for an electrical and electronic device. It has been required for
a material to be applied to have further improved a strength, an electrical conductivity,
an yield stress relaxation characteristic, a bending workability, a plating ability,
a pressing workability, a heat resisting property, or the like, in accordance with
a smaller size of an electrical and electronic device or a lighter weight in recent
years. However, it is difficult to concurrently improve properties such as the strength
and the bending workability or the strength and the electrical conductivity.
[0003] The Corson alloy is an alloy of a Cu-Ni-Si system that has a higher strength due
to a precipitation of elements such as Ni and Si. With the alloy, it is able to satisfy
characteristics required for an electrical and electronic device. However, the Corson
alloy has insufficient bending workability under a severe condition in which properties
concurrently need to be improved.
[0004] For instance, as a copper alloy with improved bending workability, there is proposed
a substance that contains Ni between 2 and 4% (by mass), Si between 0.5 mass% and
1.0 mass%, Zn between 0.1 mass% and 1.0 mass%, Al, Mn, Cr, or the like, sulfur not
more than 0.002 mass%, and a remaining portion comprised of Cu and an unavoidable
impurity. A size of a precipitate is not bigger than 10 nm, and a distribution density
of the precipitate is not lower than 1 x 105 pieces per µm3, and a hardness Hv is
not softer than 220 (refer to Japanese Patent Application Publication No.
H 06-184680). However, it is not able to obtain sufficient bending workability.
[0005] Moreover, there is proposed a copper alloy plate material that contains Ni between
4.0 mass% and 5.0 mass%, Si within a range for a ratio of Ni/Si between four and five,
and a remaining portion formed of Cu and an unavoidable impurity. An average grain
diameter of an Ni
2Si precipitate of the alloy plate material is between 3 nm and 10 nm, and an average
space of Ni
2Si precipitate is not more than 25 nm after an accelerated aging and hardening (refer
to Japanese Patent Application Publication No.
2005-089843 for instance). The alloy exhibits improved tensile strength and electrical conductivity.
Further, there is known a copper alloy that contains Ni between 0.4 mass% and 4.8
mass%, Si between 0.1 mass% and 1.2 mass%, Mg or the like approximately 0.3 mass%,
and a remaining portion formed of Cu and an unavoidable impurity. An average crystalline
grain diameter is not larger than 1 µm, and crystalline grains with a grain diameters
smaller than 3 µm occupy an area not smaller than 90% (refer to Japanese Patent Application
Publication No.
2006-089763). The copper alloy has improved tensile strength, electrical conductivity and workability.
[0006] Furthermore, Japanese Patent Application Publications No.
H06-184680, No.
2005-089843 and No.
2006-089763 have disclosed a Corson alloy in which crystalline grains are minimized in order
to improve strength. However, it has not been able to improve the electrical conductivity
and the bending workability at the same time.
DISCLOSURE OF THE INVENTION
[0007] In view of the problems mentioned above, the present inventors have examined relations
between components and compositions of a copper alloy, an average crystalline grain
diameter, a standard deviation of a crystalline grain diameter, bending workability,
or the like. As a result, it is found out that it becomes able to improve the bending
workability without deteriorating strength and electrical conductivity by properly
designing the relations. Moreover, further examinations are progressed with based
on the findings, and the present invention is completed.
[0008] According to the present invention, it becomes able to provide a copper alloy for
an electrical and electronic device and a method for producing the same as defined
below.
- 1. According to a first aspect of the present invention, a copper alloy for an electrical
and electronic device includes: Ni between 1.5 mass% and 5.0 mass%; Si between 0.4
mass% and 1.5 mass%; and a remaining portion formed of Cu and an unavoidable impurity,
wherein a mass ratio of Ni/Si is not smaller than two and not larger than seven, an
average crystalline grain diameter is not smaller than 2 µm and not larger than 20
µm, and a standard deviation of the crystalline grain diameter is not larger than
10 µm.
- 2. According to a second aspect of the present invention, in the copper alloy for
the electrical and electronic device in the first aspect, the average crystalline
grain diameter is within a range not larger than 15 µm, and the standard deviation
of the crystalline grain diameter is not larger than 8 µm.
- 3. According to a third aspect of the present invention, in the copper alloy for the
electrical and electronic device in the first aspect, the average crystalline grain
diameter is within a range not larger than 10 µm, and the standard deviation of the
crystalline grain diameter is not larger than 5 µm.
- 4. According to a fourth aspect of the present invention, the copper alloy for the
electrical and electronic device in one of the first to the third aspects further
includes at least one element between 0.005 mass% and 2.0 mass%, that is selected
from a group of Mg, Sn and Zn, and a remaining portion formed of Cu and an unavoidable
impurity.
- 5. According to a fifth aspect of the present invention, the copper alloy for the
electrical and electronic device in one of the first to the fourth aspects further
includes at least one element between 0.005 mass% and 2.0 mass%, that is selected
from a group of Ag, Co, Cr, Fe, Mn, P, Ti and Zr, and a remaining portion formed of
Cu and an unavoidable impurity.
- 6. According to a sixth aspect of the present invention, a method for producing a
copper alloy for an electrical and electronic device comprises at least the following
steps of: casting a copper alloy which includes: Ni between 1.5 mass% and 5.0 mass%;
Si between 0.4 mass% and 1.5 mass%; and a remaining portion formed of Cu and an unavoidable
impurity, wherein a mass ratio of Ni/Si is not smaller than two and not larger than
seven, and performing thereafter a hot working and then performing a cold working
(Step a); performing a process of a re-crystallization heat treatment after performing
the above defined Step a, with a temperature rising rate of not slower than 10°C per
second, to an end point temperature between 700°C and 950°C, with a retention time
between five seconds and 300 seconds, and with a cooling rate till 300°C as not slower
than 20°C per second (Step b); and performing a process of an aging precipitation
after performing the above defined Step b (Process C).
[0009] In the present invention, the average crystalline grain diameter means an average
value of the grain diameter of the individual crystals that exist in the texture of
the copper alloy after the process to be solution heated and then to be recrystallized.
Moreover, the standard deviation of the crystalline grain diameter means a value that
is evaluated with based on the individual crystalline grain diameters. Further, the
texture of the metal has a state obtained by performing the process of treating with
heat (the process to be recrystallized), or by performing the processes of treating
with heat, of aging, of annealing, or the like. It is able to observe the individual
states by an optical microscope (OM), a scanning electron microscope (SEM), or the
like.
[0010] The aspects and advantages in accordance with the present invention will be further
clarified by the following description.
BEST MODE FOR CARRYING OUT THE INVENTION
[0011] In the copper alloy in accordance with the present invention there becomes to be
improved in particular the bending workability by specifying properly the average
crystalline grain diameter of the copper alloy of Cu-Ni-Si system and the standard
deviation of the crystalline grains. And hence the alloy becomes useful for the application
to an electrical and electronic device. Next, the functions in accordance with the
component elements, the advantages and each of the contents that comprise the copper
alloy for an electrical and electronic device in accordance with the present invention
will be described in detail below.
Ni and Si contribute to an improvement of the strength by being precipitated as a
chemical compound of Ni-Si. The reason that such Ni is designed to be specified between
1.5 mass% and 5.0 mass% and that Si is designed to be specified between 0.4 mass%
and 1.5 mass% is that it is not able to obtain the strength as sufficiently if ether
one is lower than each of the lower limits, respectively, or that the strength becomes
to be saturated if ether one is higher than each of the upper limits respectively,
and also that the electrical conductivity becomes to be decreased either. Moreover,
a balance between the strength and the electrical conductivity becomes to be worsened
drastically in a case where the ratio of Ni/Si is not within the range between two
and seven. The substance is not applicable to an alloy for an electrical and electronic
device that is required to have a strength as higher and an electrical conductivity
as higher as well.
[0012] Further, regarding the copper alloy in accordance with the present invention it becomes
able to improve a material property by being contained at least any one nature of
the elements that is selected from Mg, Sn and Zn in addition to the above mentioned
alloy contents. For example in a case of adding Mg, the same contributes to an improvement
of the stress relaxation characteristic. Sn contributes to an improvement of the stress
relaxation characteristic and an enhancement of the strength as well in a case of
adding the same. Meanwhile, Zn contributes to an improvement of a plating wettability
thereon in a case of adding the same. On the contrary thereto in a case where each
of the contents of the elements is excessively lower, it is not able to obtain each
of the advantages. Still further, in a case where each of the contents is excessively
higher, such as regarding the Mg there becomes to be increased an amount of oxides
at a period of a process of casting, and then it becomes more difficult to perform
the process of casting. Still further, regarding Sn, there becomes to be a cause to
occur a crack at a period of a process of hot working, due to segregation at a period
of the process of casting. Still further, regarding Zn, it is not able to predict
any further improvement of the plating adherence thereon. Furthermore, any one of
the sample substance is not desirable due to an occurrence of a drastic decreasing
of the individual electrical conductivities respectively. Here regarding the copper
alloy in accordance with the present invention, it is able to produce simply by selecting
properly such as a condition of a process of a hot rolling, a condition of a process
of a cold rolling, a condition of a process of a treating with heat to be recrystallized,
a condition of a process of a treating with heat for aging, a condition of a final
rolling, or the like.
[0013] Moreover, it becomes able to further improve the material property by being contained
as preferably at least any one nature of the elements that is selected from a group
of Ag, Co, Cr, Fe, Mn, P, Ti and Zr in addition to the above mentioned alloy contents
in the above mentioned alloy. For example in a case of adding any one of Ag, Co and
Cr, each of the elements contributes to an improvement of the bending workability
and the strength, due to an effect of suppressing the grain diameters from becoming
rougher and larger at a period of a process of treating with heat to be crystallized,
because of being formed a chemical compound. While, any one of Fe, Ti and Zr contributes
to an improvement of the strength in a case of adding each of the same, because of
being formed a chemical compound. Meanwhile, phosphorus contributes to suppress an
amount of any of oxides at a period of a process of casting in a case of adding the
same. Further, Mn contributes to an improvement of the workability of a hot working
in a case of adding the same. On the contrary thereto in a case where each of the
contents of the elements is excessively lower, it is not able to obtain each of the
advantages. Still further, in a case where each of the contents is excessively higher,
regarding Ag, there becomes to bring about a problem from a point of view of manufacturing
cost on the production. Still further, regarding Co, it is not able to predict any
further improvement of the material property, due to the further difficulty of performing
the process of treating with heat as sufficiently in order to solution heat the same.
Still further, Cr gives rise to a saturation of the effect of suppressing the crystalline
grain diameter from rougher and larger. Still further, Fe gives rise to a decrease
of the electrical conductivity. Still further, one of Ti and Zr gives rise to a further
difficulty of casting, or the same becomes a cause for a crack to be occurred at the
period of the process of hot working, due to an amount of any of oxides as excessively
larger at a period of a process of casting. Still further, Mn gives rise to a decrease
of the electrical conductivity either. Still further, phosphorus gives rise to a deterioration
of the bending workability due to an increase of the precipitate. Furthermore, any
one of the sample substances is not desirable due to an occurrence of a drastic decreasing
of the individual electrical conductivities respectively. Here regarding the copper
alloy in accordance with the present invention, it is able to produce simply by selecting
properly such as a condition of a process of a hot rolling, a condition of a process
of a cold rolling, a condition of a process of a treating with heat to be recrystallized,
a condition of a process of a treating with heat for aging, a condition of a final
rolling, or the like.
[0014] Next, regarding a method for producing the copper alloy for an electrical device
and an electronic device that have the average crystalline grain diameter and the
standard deviation of the crystalline grain diameter, a preferred embodiment will
be described in detail below.
Here regarding a method for producing the copper alloy in accordance with the present
embodiment, it is desirable to comprise the above defined Step a, Step b and Process
C, and it is further preferable in particular to make use of the following processes
from (1) to (10) in order.
(1) Process of casting a copper alloy which includes: Ni between 1.5 mass% and 5.0
mass%; Si between 0.4 mass% and 1.5 mass%; and a remaining portion formed of Cu and
an unavoidable impurity, wherein a mass ratio between Ni and Si as Ni/Si is not smaller
than two and not larger than seven.
(2) Process of performing a hot working and then of performing a cold working.
(3) Process of treating with heat to be recrystallized;
(3-1) Temperature rising rate: it is desirable to design the temperature rising rate
as not slower than 10°C per second to an end point temperature, or it is further preferable
to be designed as not slower than 10°C per second but not faster than 100°C per second.
(3-2) End point temperature: it is desirable to be designed between 700°C and 950°C.
(3-3) Retention time: it is desirable to be designed for between five seconds and
300 seconds.
(3-4) Cooling rate: it is desirable to be designed as not slower than 20°C per second
till 300°C for instance, or it is further preferable to be designed as not slower
than 20°C per second but not faster than 200°C per second.
(4) Process of aging precipitation:
(4-1) Condition of temperature rising: it is desirable for an end point temperature
to be between 300°C and 600°C, for an amount of time for treating to be between 0.5
hour and ten hours, for a temperature rising rate at the period to be as within a
range between 2°C and 25°C per minute from a room temperature till reaching to the
maximum temperature.
(4-2) Condition of cooling: it is desirable at the period of falling the temperature
to be performed within a range between 1 and 2°C per minute for the temperature as
not lower than 300°C at an inside of a furnace.
(5) Process of annealing for reducing distortion: it is desirable to perform a heating
with a temperature at between 250°C and 400°C and with an amount of time for between
0.5 hour and five hours, or it is desirable to perform a heating with a temperature
at between 600°C and 800°C and with an amount of time for between five seconds and
60 seconds as well.
Thus, it becomes able to obtain as efficiently the copper alloy that has the above
desirable properties. Furthermore, it is further preferable to install a process for
performing a cold working into between the above mentioned Process (4) and Process
(5), that has a rate of rolling as not higher than 30% (including zero percent).
[0015] Next, an average crystalline grain diameter of the copper alloy in accordance with
the present invention and a standard deviation of the crystalline grain diameter will
be described in detail below. Here regarding the copper alloy in accordance with the
present invention, the average crystalline grain diameter is designed to be as not
smaller than 2 µm and not larger than 20 µm. And, it is desirable to be as not larger
than 15 µm, or it is further preferable to be as not larger than 10 µm. Here in a
case where the average crystalline grain diameter is excessively smaller, there is
observed a remaining of the texture to be worked at the last process, and then thereby
there may be occurred a deterioration of bending workability as drastically. Moreover,
in a case where the average crystalline grain diameter is excessively larger on the
contrary thereto, there becomes easier to be occurred a crack thereon at a period
of bending work, and then thereby there becomes to be occurred a deterioration of
bending workability. Here the standard deviation of the average crystalline grain
diameter is designed to be as not larger than 10 µm. On the contrary thereto in a
case where the deviation is excessively larger, there becomes to be a state where
the grains individually having the larger grain diameters and the grains individually
having the smaller grain diameters are coexisting together. And then in a case where
any one of the grains individually having the larger grain diameters exists at around
a top of the bended part, there may be occurred a crack on a bended surface, or there
may be occurred a peeling of the plating off from a part at around a corrugation as
largely wrinkled that may be created at around the grain having the larger grain diameter
at a period of bending.
[0016] Thus, the copper alloy for an electrical and electronic device in accordance with
the present invention becomes to be superior in the strength, the electrical conductivity
and in the processing characteristics for the bending in particular. And then it becomes
able to apply the same as preferred to the usage for the electrical device and for
the electronic device, such as a lead frame, a connector, a terminal, a relay, a switch,
or the like. Moreover, by making use of the method for producing the same in accordance
with the present invention, it becomes able to produce further efficiently the above
mentioned copper alloy for an electrical and electronic device that has the above
mentioned superior properties. Furthermore, it becomes able to apply the method as
preferred to a mass production as well. Examples
[0017] Next, the present invention will be described in further detail below, in reference
to the following examples, however, the present invention will not be limited to any
one of the examples.
(Example 1)
[0018] There is performed an ingot of the copper alloys that individually have the compositions
as shown in the following Table 1, and then there is obtained each of the ingots that
are casted and individually have a dimension of 110 mm by 160 mm by 30 mm. Moreover,
for each of the ingots there are performed the following processes of: maintaining
at a temperature of 1000°C with an amount of time of 30 minutes approximately; performing
a work thereon by making use of a hot rolling till obtaining the thickness to be as
12 mm from the initial thickness of 30 mm; performing a quenching rapidly by a water
cooling; facing to become approximately 10 mm for the thickness in order to remove
a surface oxide film layer; and performing a cold rolling to obtain the thickness
of 0.15 mm, 0.20 mm or 0.25 mm as corresponding properly to each of the testing requirements
respectively. And hence there are assumed each of the substances as an intermediate
sample.
[0019] And then for each of the above mentioned intermediate samples there are performed
the following processes of: performing a treatment with heat to be recrystallized
at each of the temperature as shown in Table 2 with maintaining the individual temperatures
for between five seconds and 300 seconds; and then performing a cooling rapidly by
making use of the water cooling or by an oil cooling. Moreover, there is designed
for a temperature rising rate from a room temperature till reaching to the maximum
temperature to be within a range of not slower than 10°C per second. Further, there
is designed for a cooling rate to be within a range of not slower than 20°C per second
for the temperature as not lower than 300°C.
[0020] And then thereafter for each of the above mentioned samples of copper alloy there
are performed the following processes of: removing a surface oxide film layer; performing
a cold rolling as not more than 30% (including zero percent) as required respectively;
and then performing a treatment with heat to be aging precipitated at a temperature
between 450°C and 550°C with an amount of time for 120 minutes approximately. Still
further, there is designed for a temperature rising rate from a room temperature till
reaching to the maximum temperature to be within a range between 2°C per minute and
25°C per minute. Still further, there is performed thereafter a cooling process with
controlling a cooling rate to be within a range between 1°C per minute and 2°C per
minute at an inside of a furnace for the temperature as not lower than 300°C which
influences a state of the precipitation. And then thereafter for each of the samples
there are performed the following processes of: performing another cold rolling as
not more than 30% (including zero percent); and then performing an annealing for reducing
a distortion, by performing a heating with a temperature at between 250°C and 400°C
and with an amount of time for between 0.5 hour and five hours, or by performing a
heating with a temperature at between 600°C and 800°C and with an amount of time for
between five seconds and 60 seconds.
[0021] Furthermore, there is performed each of the following characteristic evaluations
regarding each of the copper alloy materials for an electrical and electronic device
as the samples (samples of copper alloy) that are individually obtained in the above
mentioned manner.
A. Electrical conductivity:
[0022] There is performed a measurement of a specific resistance by making use of a four
terminal method in a constant temperature bath which is maintained at 20°C (± 0.5°C),
and then thereby there is calculated the electrical conductivity. Moreover, there
is assumed to be as 100 mm regarding a distance between each of the terminals.
B. 0.2% Yield strength and tensile strength:
[0023] There is performed a measurement for the test pieces for the number five as pursuant
to JIS Z2201, with two pieces that are pursuant to JIS Z2241, that are cut out in
a direction as parallel to a rolling. And then there is calculated each of the average
values respectively. Moreover, there is made use of the offset method regarding the
0.2% yield strength, meanwhile, there is evaluated regarding the tensile strength
with making use of the numerical value for which the maximum tensile force is divided
by an original cross sectional area.
C. Average crystalline grain diameter and the distribution thereof (standard deviation):
[0024] At first there is performed a finishing for each of the test pieces to have individual
mirror finished surfaces for individual cut faces thereon that are in a right angle
to the rolling direction, by making use of a wet polishing and then by making use
of a buffing. And then thereafter there is performed a corrosion on the polished surfaces
for a several seconds with making use of a weak acid. Moreover, there is performed
taking some photographs by making use of an optical microscope (OM) at a magnifying
power between 50 times and 600 times and of a scanning electron microscope (SEM) at
a magnifying power between 400 times and 5000 times. And hence there is performed
a measurement for a grain diameter on the individual cut faces by making use of a
crosscut method as pursuant to JIS H0501. And then thereby there becomes to be calculated
an average grain diameter. Further, there is evaluated a standard deviation of the
grain diameters by performing the measurement for each of the grain diameters as one
by one. Still further, there is assumed a population parameter of the measurements
as to be 200 in the case of evaluating the standard deviation of the grain diameters.
Furthermore, there is performed a measurement of a grain diameter in a sample that
is before performing the rolling (that corresponds to the time when the process of
treating with heat to be recrystallized is finished) regarding the grain cannot help
but become to be flat after performing the rolling in accordance with the above mentioned
measurement of the grain diameters.
D. Evaluation of bending workability (R/t (GW), R/t (BW)) :
[0025] At first there is performed removing of an oxide film layer on a surface of the individual
samples after performing the above mentioned processes, that have individual board
thickness (t) of approximately 0.25 millimeter and have individual board widths (w)
of approximately ten millimeters. And then thereafter there is performed a bending
for each to have individual angles at each inner side of the bending as ninety degrees
respectively, for the samples with the bending in parallel to the rolling direction
(a GW hereinafter), and for the other samples with the bending in a right angle to
the rolling direction (a BW hereinafter). Moreover, there is performed an evaluation
regarding the method of the evaluation of the bending by making use of a calculation
of a ratio as R/t for which a bend radius as an R that is the minimal limit value
of which there is not occurred any one of the above mentioned minute cracks thereon
is divided by the board thickness (t). Further, there is performed a judgment regarding
an observation to confirm whether or not there is any crack thereon, by making use
of the OM at the magnifying power between 50 times and 600 times, or by making use
of the SEM at the magnifying power between 400 times and 2000 times. When the value
of R/t decreases, the bending workability is improved.
E. Adherence of the plating layer:
[0026] At first there is performed a plating of bright tin to have a thickness of approximately
1 µm on each of the test pieces that individually have the dimensions of 30 mm by
10 mm. And then thereafter there is performed a keeping warm of each of the test pieces
in an atmosphere at a temperature of approximately 150°C with an amount of time for
1000 hours. Moreover, there is performed thereafter a bending thereon with an angle
to be 180 degrees and then the same is bended again to be an initial form respectively.
Further, there is performed an observation by visually regarding a state of an adherence
between the bended part and the plating of tin thereon. Furthermore, there is performed
a further observation whether or not there is existed any peeling thereon by making
use of the OM at the magnifying power between 50 times and 200 times as required.
Here there is judged for a test piece that has an area ratio of peeling at the bending
part as from zero percent but smaller than 10% to be assumed as EXCELLENT, or for
a test piece that has the same as not smaller than 10% but smaller than 30% to be
assumed as GOOD, or for a test piece that has the same as not smaller than 30% but
smaller than 50% to be assumed as ACCEPTABLE, or for a test piece that has the same
as not smaller than 50% to be assumed as NO GOOD.
F. Stress relaxation characteristic:
[0027] There is performed a measurement under the conditions that there is maintained each
of the test pieces with an amount of time for 1000 hours in a constant temperature
bath of 150°C approximately, and that there is set a load stress for a surface maximum
stress thereon to have a value as an 80% of each of the yield strengths respectively,
by adopting a cantilever block method that is pursuant to the standard specification
of Electronic Material Association of Japan (EMAS-3003).
Here regarding each of the results in accordance with the above mentioned measurements,
there is shown in Table 1 for each of the alloy compositions regarding each of the
intermediate samples, and there is shown in Table 2 through Table 4 for each of the
results of the characteristic evaluations regarding each of the above mentioned alloy
test pieces in accordance with the copper alloy samples.
[0028] (Table 1-1)

[0029] (Table 1-2)

[0030] (Table 2)

[0031] Here in accordance with Table 2, for the samples of the copper alloy 1 and 2 there
are added Ni and Si as the contents in the copper alloy respectively. While, for the
samples of the copper alloy 3 through 5 there is added any one nature of the elements
of Mg, Sn and Zn in addition to Ni and Si respectively. Moreover, for the samples
of the copper alloy 6 through 10 there are added at least any two natures of the elements
of Mg, Sn and Zn in addition to Ni and Si respectively. Further, in the samples of
the copper alloy 11 and 12 there is remained a part that the crystalline grain diameter
becomes to be excessively larger due to the temperature to be recrystallized as excessively
higher, or that is not recrystallized due to the temperature to be recrystallized
as excessively lower. Furthermore, in the samples of the copper alloy 13 through 18
the amount of addition of any one of Mg, Sn and Zn is not within the range of the
specification.
[0032] According to the result shown in Table 2, it is able to judge that both of the samples
of the copper alloy 11 and 12 as the comparative samples in which each of the crystalline
grain diameters becomes to be excessively larger are not sufficient on a practical
use due to the plating adherence thereon, the stress relaxation characteristic and
the bending workability as inferior thereto.
Moreover, it is found out on the contrary thereto that each of the copper alloys in
accordance with the present invention (the samples of the copper alloy 1 through 10,
and 13 through 15) has the characteristics of alloy as sufficient on the practical
use regarding each of the items of the evaluation. Further, it is found out as shown
in the results of the copper alloy samples 7, 8, 9 and 10 in particular that there
becomes to be improved the plating adherence thereon and also there becomes to be
contributed on the improvement of the tensile strength in the case where Zn is designed
to be added as the further alloy content. Still further, it is found out as shown
in the results of the copper alloy samples 6, 8, 9 and 10 that there becomes to be
improved the stress relaxation characteristic in the case where Mg is designed to
be added. Still further, it is found out as shown in the results of the copper alloy
samples 6, 7, 9 and 10 that there becomes to be improved the stress relaxation characteristic
as well in the case where Sn is designed to be added, and then the characteristic
is remarkable in particular regarding the copper alloy samples 9 and 10 for which
Mg is designed to be added together at the same time. Still further, it is found out
as shown in the results of the copper alloy samples 9 and 10 that there becomes to
be improved in total of the tensile strength, the stress relaxation characteristic
and the plating adherence thereon due to the addition of Mg, Sn and Zn together at
the same time. Still further, it is found out that the improvement and then the advantages
due to the above mentioned any additions of Mg, Sn and Zn will not be appeared in
a case where the amount of any of the additions is excessively smaller (refer to the
copper alloy samples 13 through 15).
[0033] Further, in a case when Mg, Sn and Zn is added excessively, it is found out that
it is difficult for casting in the case of MG (refer to the copper alloy sample 16),
and electrical conductivity drastically decreases in the case of Sn and Zn (refer
to the copper alloy samples 17 and 18).
[0034] (Table 3)

[0035] Here in accordance with Table 3, there are shown for the case where the ratio of
Ni/Si is 4.1 as the copper alloy samples 19 through 22, meanwhile, there are shown
for the case where the ratio of Ni/Si is between two and seven as the copper alloy
samples 23 through 26. Moreover, in order to compare and refer with making use of
the above mentioned classification in accordance with Table 3, the table further includes
some of the results as shown in Table 2 as well. Further, there are shown regarding
Comparative samples as the copper alloy samples 27 through 34, in which either one
of the contents of Ni and Si or the mass ratio is not within the range of the specification.
[0036] Here there are compared between the samples that individually contain Ni having the
concentration as similar to therebetween. As comparing between the copper alloy samples
23 (Example) and of the number as 30 (Comparative example), or between the copper
alloy samples 25 (Example) and of the number as 34 (Comparative example) for instance,
the individual samples in accordance with Comparative example are inferior thereto
in the tensile strength, in the 0.2% yield strength and in the electrical conductivity
respectively. Moreover, as comparing and referring between the copper alloy samples
24 (Example) and of the number as 29 (Comparative example), or between the copper
alloy samples 26 (Example) and of the number as 33 (Comparative example), the individual
samples in accordance with Comparative example have the ratio of Ni/Si as larger than
7.0, and also each of the samples is inferior thereto in the tensile strength and
in the 0.2% yield strength either respectively. Further, in the case where the concentration
of Ni becomes to be lower than 1.5 mass% as given in accordance with the copper alloy
samples 27 and 31 for example (for both as Comparative examples), there is occurred
the deterioration of the tensile strength as drastically even in the case where the
ratio of Ni/Si is maintained properly. And hence in accordance with the above mentioned
results therefrom, it is found out that there is a tendency to occur both of the decreasing
of the electrical conductivity and the deterioration of the strength in the case where
the content of Ni or the ratio of Ni/Si is not within the range of the specification.
[0037] (Table 4)

[0038] Here the results are shown in Table 4 with comparing between the copper alloy sample
35 (Example), for which there is not performed any addition of any one element that
is selected from Ag, Co, Cr, Fe, Mn, P, Ti and Zr, and the copper alloy samples 36
through 43 (Examples) for which there is performed the addition of any one of the
above mentioned elements that is selected within the range of the specification, and
the copper alloy samples 44 through 51 (Comparative examples) for which there is performed
the addition of any one of the above mentioned elements that is selected with the
amount as less than the range of the specification. And hence in accordance with the
results with the comparison therebetween, it is found out that there becomes to be
improved the tensile strength and the 0.2% yield strength due to a function caused
by the addition of the above selected any one of the elements in accordance with the
copper alloy samples 36 through 43 (for instance, such as there is precipitated the
chemical compound of the above selected any one of the elements with Ni or with Si,
or the like). And in particular regarding the copper alloy samples 37, 38, 42 and
43, it is considered that there becomes able to be controlled the characteristic of
the growth of the crystalline grains due to the addition of Co, Cr, Ti and Zr. As
a result, it is found out that there becomes to be further improved the bending workability.
Moreover, in the case where the amount of addition of the above mentioned any one
of the elements that is selected is excessively lower on the contrary thereto, it
is found out that it is not able to obtain any one of the above mentioned improvements
and the advantages (refer to the copper alloy samples 44 through 51).
[0039] Further, in accordance with the copper alloy samples 52 through 59, it is designed
to have individually the amount of addition of the above mentioned any one of the
elements that is selected as excessively larger (as Reference examples). And hence
in accordance with such as the copper alloy sample 53 for instance, it is not able
to perform the hot working due to the occurrence of the cracks thereon. Still further,
in accordance with the copper alloy samples 54, 58 and 59, it is not able to obtain
any one of samples due to the occurrence of the oxides to be generated as a large
amount at the period of the process of the casting. Furthermore, in accordance with
the copper alloy samples 52, 55, 56 and 57, there becomes to be decreased the electrical
conductivity as drastically or there becomes to be deteriorated the bending workability,
because there becomes to be increased the precipitation due to the increasing of the
amount of the additions.
[0040] (Table 5)

[0041] There are shown in Table 5 regarding the examples in the case of changing the temperature
rising rate at the period of the process of treating with heat to be recrystallized,
the end point temperature (temperature to be recrystallized), the retention time and
the cooling (temperature falling) rate. And hence in accordance with such as the copper
alloy samples 69 through 74 (Comparative examples) for instance, there are obtained
the individual bending workability as inferior due to such as the average crystalline
grain diameter becoming to be larger, or the like, because the amount of time for
the process becomes to be longer in the temperature range at which the grain becomes
to be grown. Moreover, in accordance with the copper alloy sample 68 (Comparative
example), there are worsened the tensile strength and the 0.2% yield strength, for
which the retention time is excessively shorter. Furthermore, the copper alloy samples
60 through 67 (Examples) on the contrary thereto, that there are performed the process
individually by making use of the temperature rising rate, the retention time and
the temperature falling rate within the specification of the method for producing
the copper alloy in accordance with the present invention, it is found out that it
becomes able to obtain each of the characteristics of alloy for each of Examples to
be as excellent regarding each of the items of the evaluation.
INDUSTRIAL APPLICABILITY
[0042] The copper alloy for an electrical and electronic device in accordance with the present
invention becomes to be applicable as preferred to the usage for the electrical device
and for the electronic device, such as a lead frame, a connector, a terminal, a relay,
a switch, or the like. Moreover, the method for producing the same in accordance with
the present invention becomes to be preferable as the method by which it becomes able
to produce further efficiently the above mentioned copper alloy for an electrical
and electronic device.
[0043] Thus, there is described as above regarding the present invention in reference to
the embodiment, however, the present invention will not be limited to every detail
of the description as far as a particular designation, and it should be interpreted
widely without departing from the spirit and scope of the present invention as disclosed
in the attached claims.
[0044] Furthermore, the present invention claims the priority based on Japanese Patent Application
No.
2007-080266, filed in Japan on the twenty-sixth day of March 2007, and on Japanese Patent Application
No.
2008-079256, that is filed in Japan on the twenty-fifth day of March 2008, and the entire contents
of which are expressly incorporated herein by reference.