US20090183803A1 - Copper-nickel-silicon alloys - Google Patents

Copper-nickel-silicon alloys Download PDF

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US20090183803A1
US20090183803A1 US12/336,731 US33673108A US2009183803A1 US 20090183803 A1 US20090183803 A1 US 20090183803A1 US 33673108 A US33673108 A US 33673108A US 2009183803 A1 US2009183803 A1 US 2009183803A1
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weight percent
alloy
yield strength
iacs
ksi
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US12/336,731
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Ralph A. Mutschler
Peter William Robinson
Derek E. Tyler
Andrea Kaufler
Hans-Achim Kuhn
Uwe Hofmann
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Wieland Werke AG
GBC Metals LLC
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Wieland Werke AG
GBC Metals LLC
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Priority to US12/336,731 priority Critical patent/US20090183803A1/en
Priority to MX2010006990A priority patent/MX2010006990A/en
Priority to EP08864853.0A priority patent/EP3158095B1/en
Priority to JP2010539878A priority patent/JP2011508081A/en
Priority to KR1020107016153A priority patent/KR20100120644A/en
Priority to TW097149976A priority patent/TWI461548B/en
Priority to CN2008801252801A priority patent/CN101939452A/en
Priority to PCT/US2008/087705 priority patent/WO2009082695A1/en
Priority to ES08864853.0T priority patent/ES2670425T3/en
Priority to CA2710311A priority patent/CA2710311A1/en
Publication of US20090183803A1 publication Critical patent/US20090183803A1/en
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper
    • C22C9/06Alloys based on copper with nickel or cobalt as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/08Changing 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

  • This invention relates to copper base alloys, and in particular to copper-nickel-silicon base alloys.
  • Copper-nickel-silicon base alloys are widely used for the production of high strength, electrically conductive parts such as connectors and lead frames.
  • C7025 developed by Olin Corporation, is an important example of a copper-nickel-silicon base alloy that provides good mechanical (yield strength 95 ksi -110 ksi) and good electrical properties (35% IACS) . See U.S. Pat. Nos. 4,594,221 and 4,728,372, incorporated herein by reference. More recently, C7035, a cobalt modified copper, nickel, silicon alloy, has been developed by Olin Corporation and Wieland Werke, which can provide even better mechanical (yield strength 100 ksi -130 ksi) and electrical properties (40-55% IACS). See U.S. Pat. No. 7,182,823, incorporated herein by reference.
  • the properties of copper alloys that can be important include formability, conductivity, strength, ductility, and resistance to stress relaxation.
  • Formability is typically evaluated by a bend test where copper strips are bent 90° around a mandrel of known radius.
  • a roller bend test employs a roller to form the strip around the mandrel.
  • a v-block test uses the mandrel to push the strip into an open die, forcing it to conform to the radius of the mandrel.
  • the minimum bend radius is the smallest radius mandrel around which a strip can be bent without cracks visible at a magnification of 10 ⁇ to 20 ⁇ .
  • mbr/t is reported for both good way bends, defined as the bend axis is normal to the rolling direction, and for bad way bends, defined as the bend axis is parallel to the rolling direction.
  • An mbr/t of up to 4 t for both good way bends and bad way bends is deemed to constitute good formability. More preferred is an mbr/t of up to 2.
  • IACS International Annealed Copper Standard that assigns “pure” copper a conductivity value of 100% IACS at 20° C. Throughout this disclosure, all electrical and mechanical testing is performed at room temperature, nominally 20° C., unless otherwise specified. The qualifying expression “about” indicates that exactitude is not required and should be interpreted as +/ ⁇ 10% of a recited value.
  • Strength is usually measured as yield strength.
  • a high strength copper alloy has a yield strength in excess of 95 ksi (655.1 MPa) and preferably in excess of 110 ksi (758.5 MPa). As the gauge of the copper alloy formed into components decreases and as miniaturization of these components continues, a combination of strength and conductivity for a given temper will be more important than either strength or conductivity viewed alone.
  • Ductility can be measured by elongation.
  • One measure of elongation is A10 elongation, which is the permanent extension of the gauge length after fracture, expressed as a percentage of the original gauge length L 0 where L 0 is taken equal to 10 mm.
  • Acceptable resistance to stress relaxation is viewed as at least 70% of an imparted stress remaining after a test sample is exposed to a temperature of 150° C. for 3000 hours and at least 90% of an imparted stress remaining after a test sample is exposed to a temperature of 105° C. for 1000 hours.
  • Stress relaxation may also be measured by a lift-off method as described in ASTM (American Society for Testing and Materials) Standard E328-86.
  • ASTM American Society for Testing and Materials
  • This test measures the reduction in stress in a copper alloy sample held at fixed strain for times up to 3000 hours.
  • the technique consists of constraining the free end of a cantilever beam to a fixed deflection and measuring the load exerted by the beam on the constraint as a function of time at temperature. This is accomplished by securing the cantilever beam test sample in a specially designed test rack.
  • the standard test condition is to load the cantilever beam to 80% of the room temperature 0.2% offset yield strength. If the calculated deflection exceeds about 0.2 inch, the initial stress is reduced until the deflection is less than 0.2 inch and the load is recalculated.
  • the test procedure is to load the cantilever beam to the calculated load value, adjust a threaded screw in the test rack to maintain the deflection, and locking the threaded screw in place with a nut.
  • the load required to lift the cantilever beam from the threaded screw is the initial load.
  • the test rack is placed in a furnace set to a desired test temperature.
  • the test rack is periodically removed, allowed to cool to room temperature, and the load required to lift the cantilever beam from the threaded screw is measured.
  • the percent stress remaining at the selected log times is calculated and the data are plotted on semi-log graph paper with stress remaining on the ordinate (vertical) and log time on the abscissa (horizontal). A straight line is fitted through the data using a linear regression technique. Interpolation and extrapolation are used to produce stress remaining values at 1, 1000, 3000, and 100,000 hours.
  • the resistance to stress relaxation is orientation sensitive and may be reported in the longitudinal (L) direction where 0° testing is conducted with the long dimension of the test sample in the direction of strip rolling and the deflection of the test sample is parallel to the strip rolling direction.
  • the resistance to stress relaxation may be reported in the transverse (T) direction where 90° testing is conducted with the long dimension of the test sample perpendicular to the strip rolling direction and the deflection of the test sample is perpendicular to the strip rolling direction.
  • Table 1 shows the mechanical and electrical properties of some of the commercially available copper alloys of which the inventors are aware:
  • beryllium coppers can provide high strength, because of their beryllium content, they are not suitable for many applications.
  • high strength e.g., yield strength above about 130 ksi
  • One aspect of the present invention is an age-hardening copper-nickel-silicon base alloy that can be processed to make a commercially useful strip product for use in electrical connectors and interconnections for the automotive and multimedia industries, in particular, and for any other applications requiring high yield strength and moderately high electrical conductivity in a strip, plate, wire or casting.
  • Another aspect of the present invention is a processing method to make a commercially useful strip product for use in electrical connectors and interconnections for the automotive and multimedia industries and any other applications requiring high yield strength and moderately high electrical conductivity.
  • a copper-nickel-silicon base alloy having an improved combination of yield strength and electrical conductivity that consists essentially of between about 1.0 and about 6.0 weight percent Ni, up to about 3.0 weight percent Co, between about 0.5 and about 2.0 weight percent Si, between about 0.01 and about 0.5 weight percent Mg, up to about 1.0 weight percent Cr, up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities.
  • This alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 32% IACS.
  • a copper base alloy having an improved combination of yield strength and electrical conductivity that consists essentially of: between about 3.0 and about 5.0 weight percent Ni; up to about 2.0 weight percent Co; between about 0.7 and about 1.5 weight percent Si; between about 0.03 and about 0.25 weight percent Mg; up to about 0.6 weight percent Cr; up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities.
  • This alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 32% IACS.
  • a copper-nickel-silicon base alloy having an improved combination of yield strength and electrical conductivity that consists essentially of: between about 3.5 and about 3.9 weight percent Ni; between about 0.8 and about 1.0 weight percent Co; between about 1.0 and about 1.2 weight percent Si; between about 0.05 and about 0.15 weight percent Mg; up to about 0.1 weight percent Cr; up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities.
  • This alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 32% IACS.
  • the alloys are preferably processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 38% IACS, more preferably to have a yield strength of at least about 143 ksi, and an electrical conductivity of at least about 37% IACS, and most preferably to have a yield strength of at least about 157 ksi, and an electrical conductivity of at least about 32% IACS.
  • the ratio of (Ni+Co)/(Si ⁇ Cr/5) is preferably between about 3 and about 7, and more preferably between about 3.5 and about 5.0.
  • the Ratio of Ni/Co is preferably between about 3 and about 5.
  • the alloys and processing methods of the various embodiments provide copper base alloys having an improved combination of yield strength and electrical conductivity, and preferably stress relaxation resistance as well.
  • the alloys have higher strength and greater resistance to stress relaxation than previously achieved with Cu—Ni—Si alloys, while maintaining reasonable levels of conductivity.
  • FIG. 1 is a flow chart of the treatment of the alloys in Example 1;
  • FIG. 2 is a flow chart of the treatment of the alloys in Example 2;
  • FIG. 3 is a flow chart of the treatment of the alloys in Example 3.
  • FIG. 4 is a graph of the yield strength versus conductivity for the alloys of Example 3.
  • FIG. 5 is a graph of yield strength versus bend formability (MBR/t) for the alloys of Example 3;
  • FIG. 6 is a flow chart of the treatment of the alloys of Example 4.
  • FIG. 7 is a graph of yield strength versus conductivity for the alloys of Table 5 processed by a SA-CR-age-CR-age process of Example 4;
  • FIG. 8 is a graph of yield strength versus bend formability (MBR/t) for the alloys of Table 5 processed by SA-CR-age-CR-age process of Example 4;
  • FIG. 9 is flow chart of the treatment of the alloys in Example 5.
  • FIG. 10 is a graph of yield strength vs Ni/Co ratio for alloys without chromium having similar alloying levels of Example 5;
  • FIG. 11 is flow chart of the treatment of the alloys in Example 6;
  • FIG. 12 is a flow chart of the treatment of the alloys in Example 7.
  • FIG. 13 is a graph showing the effect of stoichiometric ratio on yield strength in copper-nickel-chromium-silicon alloys from Example 7;
  • FIG. 14 is a graph showing the effect of stoichiometric ratio on yield strength in copper-nickel-cobalt-silicon alloys from Example 7;
  • FIG. 15 is a graph showing the effect of effect of stoichiometric ratio on yield strength in copper-nickel-chromium-cobalt-silicon alloys from Example 7;
  • FIG. 16 is a graph showing the effect of stoichiometric ratio on electrical conductivity in copper-nickel-chromium-silicon alloys from Example 7;
  • FIG. 17 is a graph showing the effect of stoichiometric ratio on electrical conductivity in copper-nickel-cobalt-silicon alloys from Example 7;
  • FIG. 18 is a graph showing the effect of stoichiometric ratio on electrical conductivity in copper-nickel-chromium-cobalt-silicon alloys from Example 7;
  • FIG. 19 is a flow chart of the treatment of the alloys in Example 8.
  • FIG. 20 is a graph showing the effect of stoichiometric ratio on % IACS in Example 8 alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages.
  • FIG. 21 is a graph showing the effect of stoichiometric ratio on yield strength in Example 8 alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages;
  • FIG. 22 is a flow chart of the treatment of the alloys in Example 9
  • FIG. 23 is a schematic diagram of tapered edge hot rolling specimen
  • FIG. 24 is a photograph of hot rolled K224 (without Cr), showing large edge cracks
  • FIG. 25 is a photograph of hot rolled K225 (0.11 Cr), showing no edge cracks
  • FIG. 26A is photograph of the results from tool wear testing of non-Cr alloy RN033407.
  • FIG. 26B is a photograph of the Result from tool wear test of Cr-containing alloy RN834062;
  • FIG. 27 is a flow chart of the treatment of the alloys in Example 10.
  • FIG. 28 is a graph showing the effect of stoichiometric ratio on % IACS in Example 8 and Example 10 (low Cr and Mn) alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages;
  • FIG. 29 is a graph showing the effect of stoichiometric ratio on yield strength in Example 8 and Example 10 (low Cr and Mn) alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages;
  • FIG. 30 is a flow chart of the treatment of the alloys in Example 11.
  • FIG. 31 is a flow chart of the treatment of the alloys in Example 12.
  • FIG. 32 is a flow chart of the treatment of the alloys in Example 13;
  • FIG. 33 is a flow chart of the treatment of the alloys in Example 14.
  • FIG. 34 is a flow chart of the treatment of the alloys in Example 15;
  • FIG. 35 is a flow chart of the treatment of the alloys in Example 16.
  • FIG. 36 is a graph of 90° V-block-MBR/t BW versus yield strength for alloys and processes of Examples 13, 14, 15, and 16;
  • FIG. 37 is a graph of % IACS versus yield strength for alloys and processes of Examples 13, 14, 15, and 16.
  • Alloys that are used for multimedia interconnects require high strength to avoid damage during connector insertion and to maintain good contact force while in service.
  • good but not especially high electrical conductivity is all that is required, since the conductivity merely needs to be enough to carry a signal current, and need not be the high levels needed to avoid excessive I 2 R heating in higher power applications.
  • alloy compositions of the preferred embodiments of this invention, and the scheme used to process to the finish tempers surprisingly provide highly desirable combination of properties for meeting the needs of both automotive and multimedia applications, namely very high strength along with moderately high conductivity.
  • the alloys of the preferred embodiments of the present invention are capable of being processed to strip products with combinations of yield strength/electrical conductivity of at least about 137 ksi with a conductivity of at least about 38% IACS, more preferably a yield strength of at least about 143 ksi, with a conductivity of at least about 37% IACS, and most preferably a yield strength of about 157 ksi, with a conductivity of at least about 32% IACS.
  • the alloys of the preferred embodiment of the present invention have an improved combination of yield strength and electrical conductivity, good stress relaxation resistance, along with modest levels of bendability, consist essentially of from about 1.0 to about 6.0 weight percent nickel, from about 0.5 to about 2.0 weight percent silicon, from 0.0 to about 3.0 weight percent cobalt, from about 0.01 to about 0.5 weight percent magnesium, from 0.0 to about 1.0 weight percent chromium, and from 0.0 to about 1.0 weight percent of each of tin and manganese, the balance of the alloy being copper and impurities.
  • the alloy consists essentially of from about 3.0 to about 5.0 weight percent nickel, from about 0.7 and about 1.5 weight percent silicon, from 0.0 to about 2.0 weight percent cobalt, from about 0.03 to about 0.25 weight percent magnesium, from about 0.0 to about 0.6% weight percent chromium, and from 0.0 to 1.0 weight percent of each of tin and manganese, the balance being copper and impurities.
  • an optimum level of yield strength and electrical conductivity is needed, e.g.
  • the most preferred alloy ranges are from about 3.5 to about 3.9 weight percent nickel; from about 1.0 to about 1.2 weight percent silicon; from about 0.8 to about 1.0 weight percent cobalt, from about 0.05 to about 0.15 weight percent magnesium, from 0 to about 0.1 weight percent chromium, and from 0.0 to about 1.0 weight percent of each of tin and manganese, the balance being copper and impurities.
  • excessive coarse second phases are present when alloying elements are substantially beyond the indicated upper limits.
  • the electrical conductivity and yield strength of the alloy are highest when the (Ni+Co)/(Si ⁇ Cr/S) ratio is controlled between about 3 and about 7, and more preferably between about 3.5 and about 5.
  • the ratio of Ni/Co is optimal for yield strength and conductivity when controlled between about 3 and about 5.
  • Magnesium generally increases stress relaxation resistance and softening resistance in the finished products; it also increases softening resistance during in-process aging annealing heat treatments.
  • Sn When present at low levels, Sn generally provides solid solution strengthening and also increases softening resistance during in-process aging annealing heat treatments, without excessively harming conductivity.
  • Low levels of Mn generally improve bend formability, although with a loss of conductivity.
  • the preferred embodiment of the process of the present invention comprises melting and casting; hot rolling (preferably from 750° to 1050° C.), optional milling to remove oxide, and an optional homogenization or intermediate bell anneal, cold rolling to a convenient gauge for solutionizing, solution annealing treatment (preferably at 800°-1050° C. for 10 seconds to one hour) followed by a quench or rapid cool to ambient temperature to obtain an electrical conductivity of less than about 20% IACS (11.6 MS/m) and an equiaxed grain size of about 5-20 ⁇ m; a 0 to 75% cold rolling reduction in thickness; an age hardening anneal (preferably at 300-600° C.
  • the resulting alloy can also be processed to finish gauge without using an in-process solutionizing heat treatment by using cycles of lower temperature bell annealing treatments with intervening cold work.
  • one or more optional recrystallization anneal(s) may be added to the process during the reduction from hot rolled gauge to the thickness appropriate for solutionizing.
  • the preferred scheme to result in alloy with a yield strength of at least about 140 ksi, and a conductivity of at least about 30% IACS conductivity involves solutionizing at about 900° to 1000° C., cold rolling by about 25%, aging at about 450°-500° C. for 3-9 hours, cold rolling by about 20-25% to finish gauge, and aging 300°-350° C. for 3-9 hours.
  • FIG. 1 is a flow chart of the process of this Example 1. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1′′ (1.6′′/1.35′′/1.1′′), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50′′ (0.9′′/0.7′′/0.5′′), followed by a water quench, followed by a homogenization or over-aging anneal at 590° for 6 hours.
  • the alloys were cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 2. Time and temperature were selected to achieve approximately constant grain size. The alloys were then subjected to an aging anneal of 400° to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009′′ and aged at 300° to 400° C. for 4 hours. Properties measured after the second age anneal are presented in Table 3. The data indicate that yield strength increases with increasing alloying levels in the ternary alloys J994 through J999, from 127 to 141 ksi yield strength when Si levels range from 0.8 to 1.3%, respectively.
  • Ni/Co ratio of about 3 leads to a higher strength than a Ni/Co ratio of 1 (K001 and K003), particularly at the higher Si level.
  • Mn alloys K011 and K012 show evidence that Mn substitution for Ni improves the strength/bend properties, but at a significant loss of conductivity. Sn appears to provide solid solution strengthening, when comparing J994 to K036 and K037.
  • FIG. 2 is a flow chart of the process of this Example 2. Subsequently the alloys were cold rolled 25% to 0.009′′ then subjected to an aging anneal of 400° to 500° C. for 3 hours. After an additional cold reduction of 22% to 0.007′′, samples were aged annealed at temperatures of 300° to 400° C. for 3 hours. Properties from representative conditions are listed in Table 4. Bend properties in many cases are somewhat better at similar strengths than the process in Example 1. Co (K003 and K004) and Sn (K037) additions provide the highest strength increase of the alloys in this example.
  • FIG. 3 is a flow chart of the process of this Example 3. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1′′ (1.6′′/1.35′′/1.1′′), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50′′ (0.9′′/0.7′′/0.5′′), followed by a water quench. The quenched plates were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling.
  • the alloys were then cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for 60 seconds at the temperatures listed in Table 5. The temperature was selected to maintain a fairly constant grain size. Alloys were then subjected to an aging anneal of 400° to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009′′ and aged at 300° to 400° C. for 4 hours. Properties measured after the second age anneal are presented in Table 6. From this data set, it can be observed that additions to a base Alloy of Cu—Ni—Si of Co (K068), Cr (K072), or both Co and Cr (K070) achieve the best combinations of strength, conductivity and bend formability.
  • Example 3 The alloys of Example 3 were solution heat treated in a fluidized bed furnace for 60 seconds at the temperature listed in Table 5.
  • FIG. 6 is a flow chart of the process of this Example 4. Subsequently the alloys were cold rolled 25% to 0.009′′ then subjected to an aging anneal of 400° to 500° C. for 3 hours. After an additional cold reduction of 22% to 0.007′′, samples were aged annealed at temperatures of 300° to 400° C. for 3 hours. Properties from representative conditions are listed in Table 7. Similar to Example 3, of particular note are alloys K068, K070 and K072, which show that alloys containing Co, Cr or a combination of both achieve the highest strength levels.
  • the bend formability data indicates that K068 and K070 which both contain Co have the best formability at higher strength. Yield strength is plotted against conductivity in FIG. 7 , and against bend formability in FIG. 8 . The values for alloys K068, K070 and K072 are noted.
  • FIG. 9 is a flow chart of the process of this Example 5.
  • This group of alloys was based on K068, K070 and K072 from Table 5, wherein overall alloying level and Ni/Co ratio were varied while keeping the stoichiometric ratio ((Ni+Co)/(Si ⁇ Cr/5)) close to 4.2. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1′′ (1.6′′/1.35′′/1.1′′), reheated at 900° C.
  • a Ni/Co ratio of 3 to 4 provides better strength than a ratio of 5, when one compares K077 (Ni/Co ratio of 3.62) and K078 (Ni/Co ratio of 3.83) to K079 (Ni/Co ratio of 5.04), as well as comparing K080 (Ni/Go ratio of 3.32) and K081 (Ni/Co ratio of 3.93) to K082 (Ni/Co ratio of 4.89).
  • the plots of yield strength vs Ni/Co ratio in FIG. 10 illustrate this, with the exception of K085, which has a higher Si level than K083 and K084.
  • the alloys of Table 8 were solution heat treated in a fluidized bed furnace 60 seconds at the temperature listed in Table 8. Subsequently the alloys were cold rolled 25% to 0.009′′ then subjected to an aging anneal of 450 to 500° C. for 3 hours. After an additional cold reduction of 22% to 0.007′′ samples were aged annealed at temperatures of 300 to 400° C. for 3 hours. Properties from samples given first and second ages at 450° C. and 300° C., respectively, are listed in Table 10. The Co-only alloys displayed a sensitivity to overall alloying levels with this scheme which was not found in alloys containing Cr. The only Co-only alloys at 150 ksi yield strength and above were K077 and K078, while all Cr-containing alloys reached or came close to that strength level. Strength-bend properties for this process are fairly similar to those in Table 9.
  • FIG. 11 is a flow chart of the process of this Example 6.
  • the Ni-content is adjusted in order to keep a stoichiometric ratio ((Ni+Co)/(Si ⁇ Cr/5)) of close to 4.2. After soaking two hours at 900° C. they were hot rolled to 0.472′′, thereby reheated after each pass at 900° C. for 10 minutes.
  • the bar was water quenched. After trimming and milling to 0.394′′ in order to remove the surface oxide, the alloys were cold rolled to 0.0106′′ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 11. Time and temperature were selected to achieve grain sizes below 20 ⁇ m. The alloys were then subjected to an aging anneal of 450 to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.0079′′ and aged at 300 or 400° C. for 3 hours. Properties measured after the second age anneal are presented in Table 12. The formability was measured via V-block.
  • a group of alloys was cast and processed using once more the basic compositions of K068 (Co only), K070 (Co and Cr) and K072 (Cr only) from Table 5 as a base, but in this case with a gradual drop in Si levels, thus increasing the (Ni+Co)/(Si ⁇ Cr/5) stoichiometric ratio above the 3.6 to 4.2 range of previous alloys.
  • Ni and Co levels were designed to be constant for each of the three alloy types.
  • a series of ten pound laboratory ingots with the compositions listed in Table 11 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4′′ ⁇ 4′′ ⁇ 1.75′′.
  • K143 to K146 are variants of K072, K160 to K163 variants of K070, and K164 to K167 are variants of K068.
  • FIG. 12 is a flow chart of the process of this Example 7. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1′′ (1.6′′/1.35′′/1.1′′), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50′′ (0.9′′/0.7′′/0.5′′), followed by a water quench. The quenched plates were then soaked at 5900° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling.
  • the alloys were then cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for 60 seconds at the temperatures listed in Table 13. The temperature was selected to maintain a fairly constant grain size. The alloys were then cold rolled 25% to 0.009′′ and aged 450, 475 and 500° C. for 3 hours. Properties after each aging temperature for alloys of the current example, as well as K068, K070, K072, K078, K087 and K089 are listed in Table 14. For each alloy type, yield strength decreases as the stoichiometric ratio increases above about 4.5, and fails below 120 ksi at a ratio of around 5.5. This is shown in FIGS.
  • Example 7 450° C. age 475° C. age 500° C. age alloy YS, ksi % IACS 90° bends YS, ksi % IACS 90° bends YS, ksi % IACS 90° bends K143 138.9 31.2 2.9/2.0 135.8 33.7 2.0/2.7 126.3 35.8 2.0/2.2 K144 118.1 27.5 1.8/2.2 125.6 30.8 1.3/1.1 121.3 33.1 2.2/1.3 K145 120.8 27.3 2.0/1.3 127.5 30.3 2.2/1.3 123.5 32.6 2.2/1.8 K146 113.4 26.8 1.8/1.1 121.7 30.4 2.2/2.0 116.8 32.2 1.3/1.6 K160 127.4 29.5 2.0/3.1 133.8 34.0 2.4/1.6 122.6 39.3 1.8/1.8 K161 127.4 29.4 2.4/1.1 131.3 33.0 2.2/1.6 123.5 35.7 1.8/0.7 K16
  • FIG. 19 is a flow chart of the process of this Example 8. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1′′ (1.6′′/1.35′′/1.1′′), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50′′ (0.9′′/0.7′′/0.5′′), followed by a water quench. The quenched plates were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling.
  • the alloys were then cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C. Grain size ranged from 6 to 12 ⁇ m. Alloys were then subjected to an aging anneal of 450 or 475° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009′′ and aged at 300° C. for 4 hours. Properties measured after the second age anneal are presented in Table 16.
  • Table 17 has properties measured after samples were solution heat treated in a fluidized bed furnace for 60 seconds at 950° C., cold rolled 25% to 0.009′′, given an aging anneal at 475° C. for 3 hours, cold rolled 22% to 0.007′′, and given a final anneal of 300° C. for 3 hours.
  • the results show the viability of a range of compositions with Si from 1.0 to 1.2%, with a Ni/Co ratio of 4, and a stoichiometric ratio (((Ni+Co)/(Si ⁇ Cr/5))) of 3.5 to 5.0.
  • FIGS. 20 and 21 which plot conductivity and yield strength data from Table 17 versus the stoichiometric ratio. These plots show yield strengths of 140 ksi or higher combined with conductivities of 25% IACS or higher are obtained for this process when the ratio is between 3.0 and 5.0. Cr was not found to influence properties significantly in the alloys of this example.
  • Example 8 TABLE 16 SA-age-CR-age process properties of Example 8 YS/TS/EI Alloy Ages % IACS ksi/ksi/% 90° MBR/t K188 450/300 29.3 149.5/156.1/2 3.3/5.2 K189 475/300 33.6 147.3/153.8/2 4.0/4.0 K204 450/300 29.7 149.6/155.1/2 4.0/5.2 K205 475/300 34.2 149.8/155.7/2 4.0/5.2 K206 475/300 35.0 147.9/153.9/2 4.0/5.3 K213 475/300 34.2 150.8/157.4/2 5.2/5.2
  • FIG. 22 is a flow chart of the process of this Example 9.
  • the ingots were then machined to have tapered edges, as illustrated schematically in FIG. 23 , to create a higher state of tensile stress at the edges. This condition is more prone to edge cracking than the standard flat edges, and thus more sensitive to alloying additions, in this case Cr.
  • the alloys were soaked for two hours at 900° C., and rolled in two passes to 1.12′′ (1.4′′/1.12′′) then water quenched.
  • Table 21 lists the normalized casting plant yield (CPY) of six Cr-containing and four non-Cr bars, where the normalized CPY is obtained as follows: First the individualized CPY is calculated as the ratio of coil milled weight to cast bar weight. Second the bar with the highest CPY, in this case RN 033410, is assigned a normalized CPY of 100%. Third the normalized CPY of all other bars is calculated by dividing the CPY of each bar by the CPY of RN033410. The normalized CPY of bars without Cr is 48-82% compares to 82-100% for the Cr-containing bars
  • FIG. 26A shows wear on a tool steel ball which was slid for 3000 linear inches (1500 inches on each side of the strip) under a 100 gm load over the strip surface with lard oil as a lubricant of a non-Cr sample (RN033407) that was plant solution annealed at 975° C., cold rolled 25% then aged a 450° C. and sulfuric acid cleaned, while FIG. 26B has a similar condition using a sample of a Cr-containing alloy (RN834062). The polished appearance of the ball shown in FIG.
  • FIG. 26 shows that the Cr-containing alloy caused much more wear, leading to a significantly larger volume of material being removed from the ball. This is seen in FIG. 26 as a much larger wear scar for the Cr-containing alloy. The larger wear scar suggests that during stamping of a sheet of the alloy into parts, a high amount of tool wear would occur.
  • a single casting run produced three bars with the composition shown in Table 21a. Casting plant yield of the bars, which was normalized similarly to the data of Table 21 where RN033410 is considered 100%, is given in Table 21b.
  • the CPY of the low-Cr bars compares favorably with the Cr-containing bars of Table 21. This is believed to be due to Cr reducing cracking during hot rolling even at these low levels.
  • RN037969 has a normalized CPY % above 100 due to the fact that the yield of this bar was higher than RN033410 in the earlier example.
  • FIG. 27 is a flow chart of the process of this Example 10.
  • Alloy K259 contains a smaller level of Cr than those alloys in Example 9, to investigate the lower limits of the beneficial effect of Cr on hot rolling.
  • Alloys K251, K254 and K260 contain low levels of Mn, to determine if Mn affects hot reliability in the alloy of this invention.
  • the ingots were then machined to have tapered edges, as illustrated schematically in FIG. 23 , to create a higher state of tensile stress at the edges.
  • the quenched bars were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling.
  • the alloys were then cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C. Alloys were then subjected to an aging anneal of 475° C. for 3 hours, designed to increase strength and conductivity.
  • the alloys were then cold rolled 25% to 0.009′′ and aged at 300° C. for 3 hours.
  • the alloys were cold rolled 25% to 0.009′′, given an aging anneal at 475° C. for 3 hours, cold rolled 22% to 0.007′′, and given a final anneal of 300° C.
  • Process A involved cold rolling to 0.012′′ and solution heat treating in a fluidized bed furnace for 60 seconds at 950° C., age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009′′, and giving a second anneal at 350° C. for 4 hours.
  • process B the metal was rolled to 0.050′′ and given an intermediate bell anneal (“IMBA”) of 575° C. for 8 hours.
  • IMBA intermediate bell anneal
  • the samples were subject to cold rolling to 0.012′′ and solution heat treating in a fluidized bed furnace for 60 seconds at 950° C., age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009′′, and giving a second anneal at 350° C. for 4 hours
  • process C The alloy was rolled to 0.024′′ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C., followed by cold rolling to 0.012′′ and a second solution heat treatment in a fluidized bed furnace for 60 seconds at 950° C.
  • the process involved age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009′′, and giving a second anneal at 350° C. for 4 hours.
  • process D cold rolling to 0.012′′ was followed by solution heat treatment in a fluidized bed furnace for 60 seconds at 950° C.
  • the alloy was cold rolled 25% to 0.009′′, given an aging anneal at 475° C. for 3 hours, cold rolled 22% to 0.007′′, and given a final anneal of 300° C. for 3 hours.
  • process E the metal was rolled to 0.050′′ and given an intermediate bell anneal of 575° C. for 8 hours. Then the samples were rolled to 0.024′′ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C., followed by cold rolling to 0.012′′ and a second solution heat treatment in a fluidized bed furnace for 60 seconds at 950° C. Subsequently, the process involved age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009′′, and giving a second anneal at 350° C. for 4 hours.
  • FIG. 31 is a flow chart of the process of this Example 12. After cold rolling to 0.012′′, samples were solution annealed in a fluidized bed furnace at temperatures of 925, 950, 975 and 1000° C. for 60 seconds. Coupons were then given age anneals at temperatures of 450, 475, 500 and 525° C. for three hours. Samples were then cold rolled to final thickness at varying reductions of 15, 25 and 35%.
  • Table 25 contains properties of samples with different solution anneal temperatures while the rest of the process was held constant. As solution temperature is increased, yield strength increases, while conductivity decreases. Additionally, bend formability worsens at the higher solution annealing temperatures, due to the large grain size developed during the 975 and 1000° C. anneals. Thus a solution annealed grain size below 20 ⁇ m is preferred.
  • the temperature of the first age is varied while the other processing variables are held constant, it is found that the highest strength levels are due to the intermediate aging temperatures, as shown for the 475 and 500° C. ages in Table 26. Also, the conductivity increased with increasing aging temperature. Thus the first age temperature can be manipulated to provide various desirable combinations of strength and conductivity.
  • Table 28 shows that the second age anneal temperature does not have a large effect on properties when the other processing variables are held constant. Conductivity was found to increase as the temperature of the second age increased, but to a small degree. Thus a wide operating range is acceptable for this step of the process.
  • Samples from the Cr-free plant-cast bar RN033407 (composition in Table 20) were rolled in the laboratory from the coil milled condition at 0.460′′ down to 0.012′′. Subsequently samples were solution heat treated in a fluidized bed furnace for 60 seconds at 900° C. Coupons were then rolled 25% to 0.009′′ and age annealed at 425, 450 and 475° C. for times of 4 and 8 hours at each temperature. Subsequently samples were cold rolled 22% to 0.007′′ and given a final anneal of 300° C. for three hours. The best combination of strength and conductivity resulted from the 450° C. for 8 hour age, with the properties from that condition and others listed in Table 28a.
  • FIG. 32 is a flow chart of the process of this Example 13. After soaking two hours at 900° C. they were hot rolled to 0.472′′, thereby reheated after each pass at 900° C. for 10 minutes. After the last pass the bar was water quenched. After trimming and milling to 0.394′′ in order to remove the surface oxide, the alloys were cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 29. Time and temperature were selected to achieve grain sizes below 20 ⁇ m.
  • the alloys were cold rolled 25% to 0.009′′ then subjected to an aging anneal of 450 and 475° C. for 3 hours.
  • Properties of samples are listed in Table 30.
  • the formability was measured via V-block. With increasing Si-content the yield strength is increasing from 121 ksi for the 1.05% Si alloy to 135 ksi for the 1.51% Si alloy. For the 1.16% Si variants Mg results in a benefit to yield strength of 5-7 ksi. Lowering the Ni/Co ratio from 11.37 to 4.98 enhances yield strength for the high Si (1.5%) alloys. Stress relaxation was tested by the ring method with a target initial stress of 0.8 times yield strength.
  • Table 31 shows the stress relaxation data for variants BV, BW and BX. Comparing BV and BW, due to Mg addition the stress relaxation resistance increases from 66.3% to 86.6% for the 150° C./1000 h condition and from 48.5% to 72.3% for the 200° C./1000 h condition. The stress relaxation resistance of the higher Si-containing BX amounts to 82.3% for the 150° C./1000 h condition and 68.7% for the 200° C./1000 h condition.
  • FIG. 33 is a flow chart of the process of this Example 14. Specimens of Example 13 were subsequently cold rolled to 0.007′′ with a cold reduction of 22%. Thereafter the samples were aged annealed at temperatures of 300° C. to 400° C. for 3 hours. Properties from samples given second ages at 300° C. are listed in Table 32. The formability was measured via V-block.
  • the highest yield strength was achieved with a first aging temperature of 450° C. With increasing Si-content the yield strength is increasing from 131 ksi for the Si 1.05% alloy to 147 ksi for the Si 1.51% alloy. For the Si 1.16% variants Mg results in a benefit to yield strength of 7-10 ksi. Lowering the Ni/Co ratio from 11.37 to 4.98 enhances yield strength for the high Si 1.5% alloys by 3 ksi. Stress relaxation was tested by the ring method with a target initial stress of 0.8 times yield strength. Table 33 shows the stress relaxation data for BV, BW and BX for the process SA-CR -1.AA 450° C.-CR -2.AA 300° C.
  • the stress relaxation resistance increases from 72.6% to 85.6% for the 150° C./1000 h condition and from 55.8% to 69.3% for the 200° C./1000 h condition.
  • the stress relaxation resistance of the higher Si-containing BX amounts to 81.1% for the 150° C./1000 h condition and 66.1% for the 200° C./1000 h condition.
  • FIG. 34 is a flow chart of the process of this Example 15. After soaking two hours at 900° C. they were hot rolled to 0.472′′, thereby reheated after each pass at 900° C.
  • the alloys were cold rolled to 0.012′′ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 34. Time and temperature were selected to achieve grain sizes below 20 ⁇ m.
  • the alloys were cold rolled 25% to 0.009′′ then subjected to an aging anneal of 450 and 475° C. for 3 hours.
  • Properties of samples are listed in Table 35.
  • the yield strength, formability measured with V-block and conductivity of the Cr-free FL and FM are similar to the Cr-containing BV and BW from Example 13, with comparable Si-content of 1.1%, Ni/Co ratio and stoichiometric ratio.
  • an addition of 0.1% Mg results in a benefit to yield strength of 7-8 ksi.
  • Table 36 shows the stress relaxation data for the processes with a solution annealing temperature of 950° C. Compared to the Cr-containing 1.16% Si samples of Example 13, BV and BW, the stress relaxation of FL and FM is slightly lower. Similar to Example 13, a Mg addition of 0.1% results in a stress relaxation increase from 64.6% to 82.7% for the 150° C./1000 h condition and from 44.3% to 69.2% for the 200° C./1000 h condition. The stress relaxation resistance of the Mg-containing, Si 1.39% variant FN amounts to 84.1% for the 150° C./1000 h condition and 65.9% for the 200° C./1000 h condition.
  • FIG. 35 is a flow chart of the process of this Example 16. Specimens of Example 15 were subsequently cold rolled to 0.007′′ with a cold reduction of 22%. Thereafter the samples were aged annealed at temperatures of 300° C. to 350° C. for 3 hours. Properties from samples given second ages at 300° C. are listed in Table 37. The formability was measured via V-block. The highest yield strength was achieved with a first aging temperature of 450° C.
  • FM shows a higher yield strength of 11 ksi in comparison to FL, that is partly ascribed to the Mg-content and partly ascribed to the slightly higher Si-content.
  • the yield strength, bendability and conductivity of the Cr-free FL and FM are similar to the Cr-containing BV and BW from example 15, with comparable Si-content, Ni/Co ratio and stoichiometric ratio.
  • Table 38 shows the stress relaxation data for FL and FM for the process SA 950° C.-CR-1.AA 450° C.-CR -2.AA 300° C.
  • the stress relaxation of FL and FM is lower by 2-3%.
  • a Mg addition of 0.1% results in a stress relaxation increase from 70.0% to 82.0% for the 150° C./1000 h condition and from 52.3% to 66.9% for the 200° C./1000 h condition.
  • the stress relaxation resistance of the Mg-containing, Si 1.39% variant FN amounts to 85.0% for the 150° C./1000 h condition and 66.4% for the 200° C./1000 h condition.
  • FIG. 36 shows the relation between 90°-minBR/t BW and yield strength for the alloys and processes of Examples 13, 14, 15, and 16. Both processes SA-CR-AA and SA-CR-AA-CR-AA form two groups with a certain formability-yield strength relation.
  • the solid lines are just a guide to the eye and mark increasing Min BR/t and increasing yield strength with higher Si-content and/or Mg-addition. There is almost no difference in yield strength and formability-yield strength relationship between the Cr-containing and Cr-free variants.
  • FIG. 37 shows the relation between % IACS and yield strength for the alloys and processes of Examples 13, 14, 15, and 16.
  • the Cr-free and the Cr-containing alloys show the same capability in achieving a conductivity of 30% IACS together with high yield strength.
  • the SA-CR-AA-CR-AA process achieves higher yield strength than the SA-CR-AA process, but at the same conductivity.

Abstract

A copper base alloy having an improved combination of yield strength and electrical conductivity consisting essentially of between about 1.0 and about 6.0 weight percent Ni, up to about 3.0 weight percent Co, between about 0.5 and about 2.0 weight percent Si, between about 0.01 and about 0.5 weight percent Mg, up to about 1.0 weight percent Cr, up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities, the alloy processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 25% IACS.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims the benefit of U.S. Provisional Patent Application Ser. No. 61/044,900, filed Apr. 14, 2008, and U.S. Provisional Patent Application No. 61/016,441, filed Dec. 21, 2007, the entire disclosures of which are incorporated herein, by reference.
  • BACKGROUND
  • This invention relates to copper base alloys, and in particular to copper-nickel-silicon base alloys.
  • Copper-nickel-silicon base alloys are widely used for the production of high strength, electrically conductive parts such as connectors and lead frames. C7025, developed by Olin Corporation, is an important example of a copper-nickel-silicon base alloy that provides good mechanical (yield strength 95 ksi -110 ksi) and good electrical properties (35% IACS) . See U.S. Pat. Nos. 4,594,221 and 4,728,372, incorporated herein by reference. More recently, C7035, a cobalt modified copper, nickel, silicon alloy, has been developed by Olin Corporation and Wieland Werke, which can provide even better mechanical (yield strength 100 ksi -130 ksi) and electrical properties (40-55% IACS). See U.S. Pat. No. 7,182,823, incorporated herein by reference.
  • The properties of copper alloys that can be important include formability, conductivity, strength, ductility, and resistance to stress relaxation.
  • Formability is typically evaluated by a bend test where copper strips are bent 90° around a mandrel of known radius. A roller bend test employs a roller to form the strip around the mandrel. Alternatively, a v-block test uses the mandrel to push the strip into an open die, forcing it to conform to the radius of the mandrel. For both tests the minimum bend radius (mbr) as a function of strip thickness (t) is then reported as mbr/t. The minimum bend radius is the smallest radius mandrel around which a strip can be bent without cracks visible at a magnification of 10× to 20×. Generally mbr/t is reported for both good way bends, defined as the bend axis is normal to the rolling direction, and for bad way bends, defined as the bend axis is parallel to the rolling direction. An mbr/t of up to 4 t for both good way bends and bad way bends is deemed to constitute good formability. More preferred is an mbr/t of up to 2.
  • Electrical conductivity is typically measured as a percentage of IACS. IACS refers to International Annealed Copper Standard that assigns “pure” copper a conductivity value of 100% IACS at 20° C. Throughout this disclosure, all electrical and mechanical testing is performed at room temperature, nominally 20° C., unless otherwise specified. The qualifying expression “about” indicates that exactitude is not required and should be interpreted as +/−10% of a recited value.
  • Strength is usually measured as yield strength. A high strength copper alloy has a yield strength in excess of 95 ksi (655.1 MPa) and preferably in excess of 110 ksi (758.5 MPa). As the gauge of the copper alloy formed into components decreases and as miniaturization of these components continues, a combination of strength and conductivity for a given temper will be more important than either strength or conductivity viewed alone.
  • Ductility can be measured by elongation. One measure of elongation is A10 elongation, which is the permanent extension of the gauge length after fracture, expressed as a percentage of the original gauge length L0 where L0 is taken equal to 10 mm.
  • Acceptable resistance to stress relaxation is viewed as at least 70% of an imparted stress remaining after a test sample is exposed to a temperature of 150° C. for 3000 hours and at least 90% of an imparted stress remaining after a test sample is exposed to a temperature of 105° C. for 1000 hours.
  • Stress relaxation resistance was measured via the ring method [Fox A.: Research and Standards 4 (1964) 480] wherein a strip of 50 mm length is clamped onto the outer radius of a steel ring initiating stress at the outer surface of the strip. With exposure to elevated temperatures elastic stresses change into plastic deformation. This process depends upon time, temperature and initial stress defined by the radius of the steel ring. Experiments were performed between 50° C./96 h and 210° C./384 h. After each annealing the remaining flexion of the strip is measured and the corresponding stress reduction calculated according to [Graves G. B.: Wire Industry 46 (1979) 421]. Using the Larson-Miller-Parameter P an extrapolation from the performed short time experiments at higher temperatures to long time experiments at lower temperatures can be done [Boegel A.: Metall 48 (1994) 872].
  • Stress relaxation may also be measured by a lift-off method as described in ASTM (American Society for Testing and Materials) Standard E328-86. This test measures the reduction in stress in a copper alloy sample held at fixed strain for times up to 3000 hours. The technique consists of constraining the free end of a cantilever beam to a fixed deflection and measuring the load exerted by the beam on the constraint as a function of time at temperature. This is accomplished by securing the cantilever beam test sample in a specially designed test rack. The standard test condition is to load the cantilever beam to 80% of the room temperature 0.2% offset yield strength. If the calculated deflection exceeds about 0.2 inch, the initial stress is reduced until the deflection is less than 0.2 inch and the load is recalculated. The test procedure is to load the cantilever beam to the calculated load value, adjust a threaded screw in the test rack to maintain the deflection, and locking the threaded screw in place with a nut. The load required to lift the cantilever beam from the threaded screw is the initial load. The test rack is placed in a furnace set to a desired test temperature. The test rack is periodically removed, allowed to cool to room temperature, and the load required to lift the cantilever beam from the threaded screw is measured. The percent stress remaining at the selected log times is calculated and the data are plotted on semi-log graph paper with stress remaining on the ordinate (vertical) and log time on the abscissa (horizontal). A straight line is fitted through the data using a linear regression technique. Interpolation and extrapolation are used to produce stress remaining values at 1, 1000, 3000, and 100,000 hours.
  • The resistance to stress relaxation is orientation sensitive and may be reported in the longitudinal (L) direction where 0° testing is conducted with the long dimension of the test sample in the direction of strip rolling and the deflection of the test sample is parallel to the strip rolling direction. The resistance to stress relaxation may be reported in the transverse (T) direction where 90° testing is conducted with the long dimension of the test sample perpendicular to the strip rolling direction and the deflection of the test sample is perpendicular to the strip rolling direction.
  • Table 1 shows the mechanical and electrical properties of some of the commercially available copper alloys of which the inventors are aware:
  • TABLE 1
    Examples of properties of currently available Be-free Cu-based alloys
    EI.
    Conductivity Yield
    Alloy Company Composition (% IACS) Strength, ksi
    C7025 Olin Brass Cu + 3.0Ni + 0.60Si + 0.15Mg >35  95-110
    EFTEC-75 Furukawa Cu + 3.2Ni + 0.65Si + 0.5Zn + 0.50Sn 25 116 
    EFTEC-23Z Furukawa Cu + 2.5Ni + 0.6Si + 0.5Zn + 0.03Ag 53 101-116
    EFTEC-97 Furukawa Cu + 2.3Ni + 0.55Si + 0.5Zn + 0.15Sn + 0.1Mg 40 110 
    EFTEC-98 Furukawa Unknown 38 104-136
    EFTEC-98S Furukawa Cu + 3.8Ni + 0.93Si + 0.48Zn + 0.18Sn + 0.13Mg + 0.3Cr 38  95-129
    K62 Wieland Cu + 0.3Cr + 0.4Ni + 0.6Sn + 0.03Ti 52 100 
    KLF-125 Kobe Steel Cu + 3.2Ni + 0.70Si + 0.3Zn + 1.25Mn 35 100 
    CAC-65 Kobe Steel Cu + 3.2Ni + 0.70Si + 1.0Zn + 0.50Sn 46 94
    MAX 251 Mitsubishi Cu + 2.0Ni + 0.50Si + 0.50Sn 45 89
    Shindo
    Max375 Mitsubishi Cu + 2.85Ni + 0.7Si + 0.5Zn + 0.5Sn + 0.015Mg 42  91-116
    KLF-1 Kobe Steel Cu + 3.2Ni + 0.70Si + 0.3Zn + 0.05Mn 55 88
    C7027 Olin Brass Cu + 2.0Ni + 0.60Si + 0.60Fe + 0.50Sn >40 >80 
    C18080/K88 Olin/Wieland Cu + 0.5Cr + 0.1Ag + 0.08Fe + 0.06Ti + 0.03Si 80 80
    C18070/K75 Wieland Cu + 0.3Cr + 0.1Ti + 0.02Si >75 70
    PMC 102 Poongsan Cu + 1.3Ni + 0.25Si + 0.05P 60 75
    C7035/K57 Olin/Wieland Cu + 1.4Ni + 1.1Co + 0.6Si >45 110-130
    NKC388 Nippon Mining Cu + 3.8Ni + 0.85Si + 0.18Mg − 0.1Mn 35-45 112-125
    HCL 305 Hitachi Cu + 2.5Ni + 0.5Si + 1.7Zn + 0.02P 42  87-102
    HCL 307 Hitachi Cu + 3.0Ni + 0.7Si + 1.7Zn + 0.3Sn + 0.02P 35 102-112
  • As good as these alloys are, and as widespread their use, there remain applications where alloys with higher strength and in particular higher strength without sacrificing other desirable properties such as conductivity, resistance to stress relaxation, and/or formability. While beryllium coppers can provide high strength, because of their beryllium content, they are not suitable for many applications. Among beryllium-free copper alloys, high strength (e.g., yield strength above about 130 ksi) is usually accompanied by significant diminishment of other desirable properties, in particular formability.
  • SUMMARY
  • One aspect of the present invention is an age-hardening copper-nickel-silicon base alloy that can be processed to make a commercially useful strip product for use in electrical connectors and interconnections for the automotive and multimedia industries, in particular, and for any other applications requiring high yield strength and moderately high electrical conductivity in a strip, plate, wire or casting. Another aspect of the present invention is a processing method to make a commercially useful strip product for use in electrical connectors and interconnections for the automotive and multimedia industries and any other applications requiring high yield strength and moderately high electrical conductivity.
  • In accordance with one preferred embodiment of this invention, a copper-nickel-silicon base alloy having an improved combination of yield strength and electrical conductivity is provided that consists essentially of between about 1.0 and about 6.0 weight percent Ni, up to about 3.0 weight percent Co, between about 0.5 and about 2.0 weight percent Si, between about 0.01 and about 0.5 weight percent Mg, up to about 1.0 weight percent Cr, up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities. This alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 32% IACS.
  • In accordance with another preferred embodiment of this invention, a copper base alloy having an improved combination of yield strength and electrical conductivity is provided that consists essentially of: between about 3.0 and about 5.0 weight percent Ni; up to about 2.0 weight percent Co; between about 0.7 and about 1.5 weight percent Si; between about 0.03 and about 0.25 weight percent Mg; up to about 0.6 weight percent Cr; up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities. This alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 32% IACS.
  • In accordance with another preferred embodiment of this invention, a copper-nickel-silicon base alloy having an improved combination of yield strength and electrical conductivity is provided that consists essentially of: between about 3.5 and about 3.9 weight percent Ni; between about 0.8 and about 1.0 weight percent Co; between about 1.0 and about 1.2 weight percent Si; between about 0.05 and about 0.15 weight percent Mg; up to about 0.1 weight percent Cr; up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and impurities. This alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 32% IACS.
  • The alloys are preferably processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 38% IACS, more preferably to have a yield strength of at least about 143 ksi, and an electrical conductivity of at least about 37% IACS, and most preferably to have a yield strength of at least about 157 ksi, and an electrical conductivity of at least about 32% IACS.
  • The ratio of (Ni+Co)/(Si−Cr/5) is preferably between about 3 and about 7, and more preferably between about 3.5 and about 5.0. The Ratio of Ni/Co is preferably between about 3 and about 5.
  • The alloys and processing methods of the various embodiments provide copper base alloys having an improved combination of yield strength and electrical conductivity, and preferably stress relaxation resistance as well. In particular the alloys have higher strength and greater resistance to stress relaxation than previously achieved with Cu—Ni—Si alloys, while maintaining reasonable levels of conductivity.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a flow chart of the treatment of the alloys in Example 1;
  • FIG. 2 is a flow chart of the treatment of the alloys in Example 2;
  • FIG. 3 is a flow chart of the treatment of the alloys in Example 3;
  • FIG. 4 is a graph of the yield strength versus conductivity for the alloys of Example 3;
  • FIG. 5 is a graph of yield strength versus bend formability (MBR/t) for the alloys of Example 3;
  • FIG. 6 is a flow chart of the treatment of the alloys of Example 4;
  • FIG. 7 is a graph of yield strength versus conductivity for the alloys of Table 5 processed by a SA-CR-age-CR-age process of Example 4;
  • FIG. 8 is a graph of yield strength versus bend formability (MBR/t) for the alloys of Table 5 processed by SA-CR-age-CR-age process of Example 4;
  • FIG. 9 is flow chart of the treatment of the alloys in Example 5;
  • FIG. 10 is a graph of yield strength vs Ni/Co ratio for alloys without chromium having similar alloying levels of Example 5;
  • FIG. 11 is flow chart of the treatment of the alloys in Example 6;
  • FIG. 12 is a flow chart of the treatment of the alloys in Example 7;
  • FIG. 13 is a graph showing the effect of stoichiometric ratio on yield strength in copper-nickel-chromium-silicon alloys from Example 7;
  • FIG. 14 is a graph showing the effect of stoichiometric ratio on yield strength in copper-nickel-cobalt-silicon alloys from Example 7;
  • FIG. 15 is a graph showing the effect of effect of stoichiometric ratio on yield strength in copper-nickel-chromium-cobalt-silicon alloys from Example 7;
  • FIG. 16 is a graph showing the effect of stoichiometric ratio on electrical conductivity in copper-nickel-chromium-silicon alloys from Example 7;
  • FIG. 17 is a graph showing the effect of stoichiometric ratio on electrical conductivity in copper-nickel-cobalt-silicon alloys from Example 7;
  • FIG. 18 is a graph showing the effect of stoichiometric ratio on electrical conductivity in copper-nickel-chromium-cobalt-silicon alloys from Example 7;
  • FIG. 19 is a flow chart of the treatment of the alloys in Example 8;
  • FIG. 20 is a graph showing the effect of stoichiometric ratio on % IACS in Example 8 alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages.
  • FIG. 21 is a graph showing the effect of stoichiometric ratio on yield strength in Example 8 alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages;
  • FIG. 22 is a flow chart of the treatment of the alloys in Example 9
  • FIG. 23 is a schematic diagram of tapered edge hot rolling specimen;
  • FIG. 24 is a photograph of hot rolled K224 (without Cr), showing large edge cracks;
  • FIG. 25 is a photograph of hot rolled K225 (0.11 Cr), showing no edge cracks;
  • FIG. 26A is photograph of the results from tool wear testing of non-Cr alloy RN033407; and
  • FIG. 26B is a photograph of the Result from tool wear test of Cr-containing alloy RN834062;
  • FIG. 27 is a flow chart of the treatment of the alloys in Example 10;
  • FIG. 28 is a graph showing the effect of stoichiometric ratio on % IACS in Example 8 and Example 10 (low Cr and Mn) alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages; and
  • FIG. 29 is a graph showing the effect of stoichiometric ratio on yield strength in Example 8 and Example 10 (low Cr and Mn) alloys processed by the SA-CR-age-CR-age approach with 475° C./300° C. ages;
  • FIG. 30 is a flow chart of the treatment of the alloys in Example 11; and
  • FIG. 31 is a flow chart of the treatment of the alloys in Example 12;
  • FIG. 32 is a flow chart of the treatment of the alloys in Example 13;
  • FIG. 33 is a flow chart of the treatment of the alloys in Example 14;
  • FIG. 34 is a flow chart of the treatment of the alloys in Example 15;
  • FIG. 35 is a flow chart of the treatment of the alloys in Example 16;
  • FIG. 36 is a graph of 90° V-block-MBR/t BW versus yield strength for alloys and processes of Examples 13, 14, 15, and 16; and
  • FIG. 37 is a graph of % IACS versus yield strength for alloys and processes of Examples 13, 14, 15, and 16.
  • DETAILED DESCRIPTION
  • There is a need in the marketplace for copper strip alloys with higher strength and electrical conductivity, along with good stress relaxation resistance. This combination of properties is particularly important for parts that are formed into various electrical interconnections for use in multimedia electrical connector and terminal applications. Commercially available copper alloys, such as C510 (phosphor bronze), C7025, C7035, C17410 and C17460 are being used in these applications for their generally favorable combinations of strength and conductivity. However, while these alloys have adequate strength for most current carrying applications, the continuing trend for miniaturization of components demands copper alloys that offer high strength in combination with reasonably good electrical conductivity and reasonably good stress relaxation resistance along with reasonable cost. It is also desirable to minimize or eliminate potentially toxic alloying elements such as beryllium.
  • Alloys that are used for multimedia interconnects require high strength to avoid damage during connector insertion and to maintain good contact force while in service. For these applications, good but not especially high electrical conductivity is all that is required, since the conductivity merely needs to be enough to carry a signal current, and need not be the high levels needed to avoid excessive I2R heating in higher power applications. For these applications, there are even more stringent requirements for mechanical stability at room and slightly elevated service temperatures, as characterized by good stress relaxation resistance at about 100° C., for example.
  • The alloy compositions of the preferred embodiments of this invention, and the scheme used to process to the finish tempers surprisingly provide highly desirable combination of properties for meeting the needs of both automotive and multimedia applications, namely very high strength along with moderately high conductivity. In particular, the alloys of the preferred embodiments of the present invention are capable of being processed to strip products with combinations of yield strength/electrical conductivity of at least about 137 ksi with a conductivity of at least about 38% IACS, more preferably a yield strength of at least about 143 ksi, with a conductivity of at least about 37% IACS, and most preferably a yield strength of about 157 ksi, with a conductivity of at least about 32% IACS.
  • The alloys of the preferred embodiment of the present invention, have an improved combination of yield strength and electrical conductivity, good stress relaxation resistance, along with modest levels of bendability, consist essentially of from about 1.0 to about 6.0 weight percent nickel, from about 0.5 to about 2.0 weight percent silicon, from 0.0 to about 3.0 weight percent cobalt, from about 0.01 to about 0.5 weight percent magnesium, from 0.0 to about 1.0 weight percent chromium, and from 0.0 to about 1.0 weight percent of each of tin and manganese, the balance of the alloy being copper and impurities. More preferably, the alloy consists essentially of from about 3.0 to about 5.0 weight percent nickel, from about 0.7 and about 1.5 weight percent silicon, from 0.0 to about 2.0 weight percent cobalt, from about 0.03 to about 0.25 weight percent magnesium, from about 0.0 to about 0.6% weight percent chromium, and from 0.0 to 1.0 weight percent of each of tin and manganese, the balance being copper and impurities. Where an optimum level of yield strength and electrical conductivity is needed, e.g. a combination of 140 ksi YS/30% IACS, the most preferred alloy ranges are from about 3.5 to about 3.9 weight percent nickel; from about 1.0 to about 1.2 weight percent silicon; from about 0.8 to about 1.0 weight percent cobalt, from about 0.05 to about 0.15 weight percent magnesium, from 0 to about 0.1 weight percent chromium, and from 0.0 to about 1.0 weight percent of each of tin and manganese, the balance being copper and impurities. Generally, excessive coarse second phases are present when alloying elements are substantially beyond the indicated upper limits.
  • The electrical conductivity and yield strength of the alloy are highest when the (Ni+Co)/(Si−Cr/S) ratio is controlled between about 3 and about 7, and more preferably between about 3.5 and about 5. The ratio of Ni/Co is optimal for yield strength and conductivity when controlled between about 3 and about 5.
  • Magnesium generally increases stress relaxation resistance and softening resistance in the finished products; it also increases softening resistance during in-process aging annealing heat treatments. When present at low levels, Sn generally provides solid solution strengthening and also increases softening resistance during in-process aging annealing heat treatments, without excessively harming conductivity. Low levels of Mn generally improve bend formability, although with a loss of conductivity.
  • The preferred embodiment of the process of the present invention comprises melting and casting; hot rolling (preferably from 750° to 1050° C.), optional milling to remove oxide, and an optional homogenization or intermediate bell anneal, cold rolling to a convenient gauge for solutionizing, solution annealing treatment (preferably at 800°-1050° C. for 10 seconds to one hour) followed by a quench or rapid cool to ambient temperature to obtain an electrical conductivity of less than about 20% IACS (11.6 MS/m) and an equiaxed grain size of about 5-20 μm; a 0 to 75% cold rolling reduction in thickness; an age hardening anneal (preferably at 300-600° C. from 10 minutes to 10 hours); and optionally a further cold rolling 10 to 75% reduction in thickness to finish gauge; and second age hardening anneal (preferably at 250 to 500° C. for 10 minutes to 10 hours). The resulting alloy can also be processed to finish gauge without using an in-process solutionizing heat treatment by using cycles of lower temperature bell annealing treatments with intervening cold work. In addition, one or more optional recrystallization anneal(s) may be added to the process during the reduction from hot rolled gauge to the thickness appropriate for solutionizing.
  • The preferred scheme to result in alloy with a yield strength of at least about 140 ksi, and a conductivity of at least about 30% IACS conductivity involves solutionizing at about 900° to 1000° C., cold rolling by about 25%, aging at about 450°-500° C. for 3-9 hours, cold rolling by about 20-25% to finish gauge, and aging 300°-350° C. for 3-9 hours.
  • While this disclosure is particularly drawn to a process for the manufacture of copper alloy strip, the alloys of the invention and the processes of the invention are equally amenable to the manufacture of other copper alloy products, such as foil, wire, bar and tube. In addition, processes other than conventional casting, such as strip casting, powder metallurgy and spray casting are also within the scope of the invention.
  • The alloys and methods of the preferred embodiments will be better understood from the following illustrative examples:
  • Example 1 Increasing Alloy Levels Increases Strength; Cobalt Substitution Improves Both Strength and Conductivity
  • A series of ten pound laboratory ingots with the compositions listed in Table 2 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. FIG. 1 is a flow chart of the process of this Example 1. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1″ (1.6″/1.35″/1.1″), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench, followed by a homogenization or over-aging anneal at 590° for 6 hours. After trimming and milling to remove the surface oxide, the alloys were cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 2. Time and temperature were selected to achieve approximately constant grain size. The alloys were then subjected to an aging anneal of 400° to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009″ and aged at 300° to 400° C. for 4 hours. Properties measured after the second age anneal are presented in Table 3. The data indicate that yield strength increases with increasing alloying levels in the ternary alloys J994 through J999, from 127 to 141 ksi yield strength when Si levels range from 0.8 to 1.3%, respectively. Comparing J994, K001 and K002 to examine the effect of Co on alloys near 0.8% Si, the substitution of Co for Ni increases both yield strength and conductivity. Considering a Co substitution for Ni in alloys with ˜1.2% Si, K003 shows a decrease in yield strength and an increase in conductivity, while K004 shows an increase in yield strength and decrease in conductivity when compared to J998.
  • Having a Ni/Co ratio of about 3 (K002 and K004) leads to a higher strength than a Ni/Co ratio of 1 (K001 and K003), particularly at the higher Si level. Mn alloys K011 and K012 show evidence that Mn substitution for Ni improves the strength/bend properties, but at a significant loss of conductivity. Sn appears to provide solid solution strengthening, when comparing J994 to K036 and K037.
  • TABLE 2
    Alloys of Examples 1 and 2
    Grain
    Solution Size,
    Alloy Analyzed composition, wt % Anneal conditions μm
    J994 Cu—3.33Ni—0.81Si  850° C. - 1 minute 11.2
    J995 Cu—3.78Ni—0.92Si  900° C. - 1 minute 16.5
    J996 Cu—4.17Ni—1.03Si  900° C. - 1 minute 22.1
    J997 Cu—4.48Ni—1.12Si  900° C. - 1 minute 22.1
    J998 Cu—4.88Ni—1.24Si  900° C. - 1 minute 12.9
    J999 Cu—5.39Ni—1.35Si  900° C. - 2 minute 14.1
    K001 Cu—1.65Ni—0.82Si—1.66Co 1000° C. - 30 seconds 12.9
    K002 Cu—2.56Ni—0.80Si—0.79Co  950° C. - 1 minute 17.7
    K003 Cu—2.45Ni—1.23Si—2.46Co 1000° C. - 30 seconds 6.7
    K004 Cu—3.70Ni—1.22Si—1.15Co 1000° C. - 30 seconds 12.9
    K009 Cu—1.74Ni—0.78Si—1.67Mn  850° C. - 30 seconds 28.2
    K010 Cu—2.65Ni—0.79Si—0.79Mn  850° C. - 30 seconds 22.1
    K011 Cu—2.51Ni—1.19Si—2.56Mn  850° C. - 1 minute 9.1
    K012 Cu—3.70Ni—1.21Si—1.19Mn  850° C. - 1 minute 9.8
    K013 Cu—3.22Ni—0.81Si—0.10Cr  850° C. - 1 minute 12.6
    K014 Cu—3.31Ni—0.82Si—0.18Cr  850° C. - 1 minute 10.7
    K015 Cu—4.82Ni—1.21Si—0.09Cr  900° C. - 1 minute 15.5
    K016 Cu—4.89Ni—1.26Si—0.18Cr  900° C. - 1 minute 12.9
    K036 Cu—3.69Ni—0.73Si—0.52Sn  850° C. - 2 minute 10.3
    K037 Cu—3.66Ni—0.77Si—0.93Sn  850° C. - 2 minute 16.2
    K040 Cu—3.74Ni—0.72Si—0.08Mg  850° C. - 2 minute 17.7
    K041 Cu—3.78Ni—0.76Si—0.205Mg  850° C. - 2 minute 18.6
  • TABLE 3
    Properties of the Alloys from Examples 1 from SA-age-CR-age process
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    J994 450/300 36.8 126.7/130.8/2 2.9/3.4
    J995 450/300 35.5 130.8/134.7/1 3.2/6.7
    J996 450/300 34.5 132.7/138.5/2 3.1/6.9
    J997 450/300 33.7 135.3/139.3/2 3.7/6.7
    J998 450/300 34.3 137.9/144.2/2 3.3/8.6
    J999 450/300 34.2 140.9/147.1/2 3.4/6.7
    K001 500/300 40.3 129.2/134.4/2
    K002 500/350 40.5 130.3/135.8/2 3.8/5.2
    K003 450/300 37.8 129.7/134.3/2 3.5/3.7
    K004 450/300 28.4 145.3/150.8/2 5.1/6.8
    K009 450/350 16.5 108.1/113.3/4
    K010 450/300 22.9 127.1/131.3/2
    K011 400/300 11.9 137.6/141.0/2 2.4/3.2
    K012 400/300 17.0 135.4/140.4/2 2.4/3.7
    K013 450/300 36.7 125.4/129.6/2
    K014 450/300 36.2 128.0/131.9/2
    K015 450/300 33.8 135.6/139.8/2 3.5/5.2
    K016 450/300 32.4 136.0/140.4/2 3.3/5.2
    K036 450/300 34.3 131.5/143.1/1 3.9/6.9
    K037 450/300 30.8 135.2/147.1/2 3.5/6.8
    K040 450/350 38.4 125.4/136.5/2
    K041 450/350 37.7 123.7/135.5/1
  • Example 2 Cobalt Improves Strength
  • Selected alloys of Example 1 were solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 2. FIG. 2 is a flow chart of the process of this Example 2. Subsequently the alloys were cold rolled 25% to 0.009″ then subjected to an aging anneal of 400° to 500° C. for 3 hours. After an additional cold reduction of 22% to 0.007″, samples were aged annealed at temperatures of 300° to 400° C. for 3 hours. Properties from representative conditions are listed in Table 4. Bend properties in many cases are somewhat better at similar strengths than the process in Example 1. Co (K003 and K004) and Sn (K037) additions provide the highest strength increase of the alloys in this example.
  • TABLE 4
    Properties of the Examples 2 from SA-CR-age-CR-age process
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    J994 450/300 38.3 130.0/134.3/2 2.3/3.7
    J997 450/300 37.7 125.2/132.7/2 2.9/8.9
    J998 400/300 28.8 128.4/134.0/2 3.1/4.0
    J999 400/300 29.5 131.9/135.4/2 3.1/5.1
    K002 450/300 35.1 125.0/129.2/1 2.4/4.9
    K003 450/300 33.7 135.2/140.3/2 3.1/4.0
    K004 450/300 31.9 134.4/139.7/2 3.7/6.7
    K014 450/300 38.1 127.9/132.3/2 2.3/4.0
    K036 450/300 36.0 129.2/131.8/1 3.1/3.9
    K037 450/300 32.0 135.2/139.8/2 3.3/4.7
    K040 450/300 38.7 127.1/129.3/1
    K041 450/300 38.4 132.4/136.4/1 3.6/4.7
  • Example 3 Cobalt and Chromium Levels and (Ni+Co)/(Si−Cr/5) Ratio
  • A series of ten pound laboratory ingots with the compositions listed in Table 5 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. FIG. 3 is a flow chart of the process of this Example 3. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1″ (1.6″/1.35″/1.1″), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench. The quenched plates were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling. The alloys were then cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for 60 seconds at the temperatures listed in Table 5. The temperature was selected to maintain a fairly constant grain size. Alloys were then subjected to an aging anneal of 400° to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009″ and aged at 300° to 400° C. for 4 hours. Properties measured after the second age anneal are presented in Table 6. From this data set, it can be observed that additions to a base Alloy of Cu—Ni—Si of Co (K068), Cr (K072), or both Co and Cr (K070) achieve the best combinations of strength, conductivity and bend formability. It is also noted that relatively high Si levels of 1.2% and above were present in the samples with the highest strength. While there was some evidence of strengthening from Sn, this was accompanied by poor bend formability. In Table 5, it can be seen that the ratio (Ni+Co)/(Si−Cr/5) is very close to 4 for most of the alloys, particularly K068, K070 and K072. Also, the Ni/Co ratio was close to 3 for K068 and K070. Yield strength is plotted against conductivity in FIG. 4, and against bend formability in FIG. 5. The values for K068, K070 and K072 are identified to show their unusually good combination of properties.
  • TABLE 5
    Alloys of Examples 3 and 4
    (Ni + Co)/ Solution Anneal Grain Size,
    Alloy Analyzed composition, wt % (Si − Cr/5) Ratio Ni/Co Temperature μm
    K056 Cu—4.94Ni—0.97Si—0.86Sn 5.09 900° C. 15
    K057 Cu—2.63Ni—0.73Co—0.80Si—0.88Sn 4.20 3.60 925° C. 16
    K058 Cu—3.80Ni—0.97Co—1.24Si—0.83Sn 3.85 3.92 950° C. 14
    K059 Cu—3.27Ni—0.82Si—0.22Mn 3.99 850° C. 20
    K061 Cu—3.83Ni—1.28Co—1.27Si—0.31Mn 4.02 2.99 950° C. 8
    K065 Cu—4.96Ni—1.25Si—0.085Mg 3.97 900° C. 17
    K066 Cu—3.29Ni—0.84Si—0.33Mn—0.092Mg 3.92 850° C. 10
    K067 Cu—2.57Ni—0.83Co—0.83Si—0.082Mg 4.10 3.10 950° C. 21
    K068 Cu—3.80Ni—1.21Co—1.27Si—0.048Mg 3.94 3.14 975° C. 12
    K069 Cu—3.42Ni—0.84Si—0.89Sn—0.062Mg 4.07 875° C. 28
    K070 Cu—3.83Ni—1.29Co—1.39Si—0.56Cr 4.01 2.97 975° C. 8
    K071 Cu—3.36Ni—0.95Si—0.54Cr—0.035Mg 3.99 950° C. 19
    K072 Cu—4.64Ni—1.28Si—0.54Cr—0.078Mg 3.96 950° C. 17
    K073 Cu—3.52Ni—1.07Si—1.06Cr—0.047Mg 4.10 950° C. 14
    K074 Cu—4.11Ni—1.31Si—1.01Cr—0.058Mg 3.71 975° C. 18
    K075 Cu—4.71Ni—1.29Si—0.50Cr—0.85Sn 3.96 950° C. 19
    K076 Cu—3.54Ni—1.00 Si—0.49Cr—0.89Sn 3.92 925° C. 17
  • TABLE 6
    Properties from SA-age-CR-age process of Example 3
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    K056 450/300 25.7 142.7/148.4/2 8.7/8.7
    K057 450/350 29.0 131.3/137.6/3 3.3/6.9
    K058 450/300 24.5 142.8/149.0/2 5.2/6.9
    K059 450/350 32.2 132.3/137.5/3 2.9/2.9
    K061 450/350 27.2 142.0/146.5/2 3.6/5.2
    K065 450/300 32.4 137.8/143.1/1 6.9/6.9
    K066 450/350 29.1 134.5/139.8/2 3.1/3.1
    K067 500/300 38.6 132.4/137.0/2 3.8/5.2
    K068 450/300 28.6 143.2/149.3/2 4.0/6.9
    K069 450/350 30.3 134.1/139.4/3 4.0/6.9
    K070 450/350 31.0 147.1/151.9/2 4.0/4.0
    K071 450/350 33.5 134.9/140.0/3 3.1/3.3
    K072 450/350 30.6 145.7/151.1/2 4.0/6.9
    K073 450/350 33.8 141.6/146.6/2 3.8/4.0
    K074 450/350 29.4 146.9/153.1/2 3.8/6.9
    K075 450/350 26.2 145.4/152.9/3 5.2/8.7
    K076 450/350 27.7 137.7/144.8/3 3.1/6.9
  • Example 4 Cobalt and Chromium for Strength and Formability
  • The alloys of Example 3 were solution heat treated in a fluidized bed furnace for 60 seconds at the temperature listed in Table 5. FIG. 6 is a flow chart of the process of this Example 4. Subsequently the alloys were cold rolled 25% to 0.009″ then subjected to an aging anneal of 400° to 500° C. for 3 hours. After an additional cold reduction of 22% to 0.007″, samples were aged annealed at temperatures of 300° to 400° C. for 3 hours. Properties from representative conditions are listed in Table 7. Similar to Example 3, of particular note are alloys K068, K070 and K072, which show that alloys containing Co, Cr or a combination of both achieve the highest strength levels. The bend formability data indicates that K068 and K070 which both contain Co have the best formability at higher strength. Yield strength is plotted against conductivity in FIG. 7, and against bend formability in FIG. 8. The values for alloys K068, K070 and K072 are noted.
  • TABLE 7
    Properties from SA-CR-age-CR-age process of the Alloys of Exhibit 4
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    K056 450/300 29.1 147.4/152.4/2 5.7/8.6
    K057 450/300 29.7 136.1/141.9/2 2.0/5.7
    K058 450/300 25.6 146.7/153.3/1 2.0/8.6
    K065 450/300 34.7 142.9/145.4/2 3.6/4.9
    K067 500/300 38.4 137.4/141.7/3 2.9/5.7
    K068 450/300 30.3 151.6/155.3/1 3.6/4.9
    K069 450/300 29.7 139.4/145.7/1 2.9/8.6
    K070 450/300 31.1 152.3/157.9/2 2.9/3.9
    K071 450/300 34.8 143.8/147.6/2 2.9/3.9
    K072 450/300 31.4 155.4/161.3/1 2.7/8.6
    K073 450/300 34.7 147.2/150.9/2 2.7/3.9
    K074 450/300 29.8 153.9/160.0/1 2.1/3.9
    K075 450/300 26.5 151.4/158.2/2  2.0/11.0
    K076 450/300 28.1 142.8/149.0/1 2.1/8.6
  • Example 5 Nickel:Cobalt Ratio
  • A series of ten pound laboratory ingots with the compositions listed in Table 8 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. FIG. 9 is a flow chart of the process of this Example 5. This group of alloys was based on K068, K070 and K072 from Table 5, wherein overall alloying level and Ni/Co ratio were varied while keeping the stoichiometric ratio ((Ni+Co)/(Si−Cr/5)) close to 4.2. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1″ (1.6″/1.35″/1.1″), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench. The quenched plates were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling. The alloys were then cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for 60 seconds at the temperature listed in Table 8. The temperature was selected to maintain a fairly constant grain size. Alloys were then subjected to an aging anneal of 450° to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009″ and aged at 300 to 400° C. for 4 hours. Properties measured after the second age anneal for the process with a 475° C. first age and 300° C. second age are presented in Table 9. For the Co-only set of compositions (K077 to K085), yield strength values tend to increase with higher alloying content. For example, K078, with a Ni+Co+Cr+Si value of 6.24, had a yield strength of 155 ksi while K084 with a Ni+Co+Cr+Si value of 5.22 had a 139 ksi yield strength. A Ni/Co ratio of 3 to 4 provides better strength than a ratio of 5, when one compares K077 (Ni/Co ratio of 3.62) and K078 (Ni/Co ratio of 3.83) to K079 (Ni/Co ratio of 5.04), as well as comparing K080 (Ni/Go ratio of 3.32) and K081 (Ni/Co ratio of 3.93) to K082 (Ni/Co ratio of 4.89). The plots of yield strength vs Ni/Co ratio in FIG. 10 illustrate this, with the exception of K085, which has a higher Si level than K083 and K084. The Co-and-Cr-containing alloys, K086 to K094, were not as sensitive to overall alloying levels and Ni/Co ratio as the Co-only alloys. The Cr-only alloys (K095 to K097) also had comparable properties to the other alloy types.
  • TABLE 8
    Alloys of Example 5
    (Ni + Co)/(Si − Solution Anneal Grain Size,
    Alloy Analyzed composition, wt % Ni/Co Ni + Co + Cr + Si Cr/5) Ratio Temperature, ° C. μm
    K077 Cu—3.84Ni—1.06Co—1.31Si 3.62 6.21 3.740 975 10.0
    K078 Cu—3.98Ni—1.04Co—1.22Si 3.83 6.24 4.115 975 10.3
    K079 Cu—4.28Ni—0.85Co—1.32Si 5.04 6.45 3.886 975 14.8
    K080 Cu—3.49Ni—1.05Co—1.10Si 3.32 5.64 4.127 975 15.5
    K081 Cu—3.77Ni—0.96Co—1.17Si 3.93 5.90 4.043 975 16.9
    K082 Cu—3.86Ni—0.79Co—1.12Si 4.89 5.77 4.152 975 20.4
    K083 Cu—3.22Ni—1.05Co—1.06Si 3.07 5.33 4.028 975 15.5
    K084 Cu—3.33Ni—0.89Co—1.00Si 3.74 5.22 4.220 950 15.3
    K085 Cu—3.59Ni—0.75Co—1.16Si 4.79 5.50 3.741 950 18.7
    K086 Cu—3.80Ni—1.20Co—1.46Si—0.57Cr 3.17 7.03 3.715 975 10.9
    K087 Cu—4.03Ni—1.01Co—1.37Si—0.60Cr 3.99 7.01 4.032 975 15.9
    K088 Cu—4.26Ni—0.82Co—1.51Si—0.57Cr 5.20 7.16 3.639 975 16.4
    K089 Cu—3.50Ni—1.11Co—1.33Si—0.58Cr 3.15 6.52 3.797 975 10.5
    K090 Cu—3.75Ni—0.92Co—1.25Si—0.55Cr 4.08 6.47 4.096 975 16.3
    K091 Cu—3.97Ni—0.79Co—1.42Si—0.56Cr 5.03 6.74 3.639 975 16.7
    K092 Cu—3.25Ni—1.01Co—1.22Si—0.58Cr 3.22 6.06 3.859 975 15.2
    K093 Cu—3.43Ni—0.86Co—1.30Si—0.51Cr 3.99 6.10 3.581 975 16.0
    K094 Cu—3.50Ni—0.73Co—1.22Si—0.59Cr 4.79 6.04 3.838 975 17.5
    K095 Cu—4.97Ni—1.36Si—0.60Cr 6.93 4.008 950 18.4
    K096 Cu—4.63Ni—1.35Si—0.61Cr 6.59 3.770 925 12.0
    K097 Cu—4.20Ni—1.18Si—0.59Cr 5.97 3.955 925 18.9
  • TABLE 9
    Properties from SA-age-CR-age process of Example 5
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    K077 475/300 29.1 152.1/159.3/4 5.2/5.2
    K078 475/300 29.7 155.5/162.3/4 5.2/5.2
    K079 475/300 30.7 143.7/150.1/4
    K080 475/300 31.2 142.4/147.9/3 5.2/3.6
    K081 475/300 30.7 144.2/148.3/3 4.0/6.1
    K082 475/300 32.2 137.7/142.7/2
    K083 475/300 31.1 140.0/145.8/3 5.2/5.2
    K084 475/300 32.1 138.9/145.6/3
    K085 475/300 31.8 140.4/146.3/2
    K086 475/300 30.1 151.6/157.9/4 5.2/6.1
    K087 475/300 30.5 149.4/153.6/3 5.2/3.6
    K088 475/300 30.4 152.2/159.3/4 5.2/5.2
    K089 475/300 30.3 149.0/155.6/3 4.0/5.2
    K090 475/300 31.3 151.9/157.4/3 5.2/3.8
    K091 475/300 30.7 149.5/154.5/3 5.2/6.1
    K092 475/300 30.8 146.5/152.1/3 4.0/5.2
    K093 475/300 30.3 147.2/153.4/4 5.2/5.2
    K094 475/300 31.2 148.1/154.4/2 4.0/3.8
    K095 475/300 30.7 150.2/159.1/3 3.8/6.1
    K096 475/300 32.1 153.3/160.6/4 4.0/6.1
    K097 475/300 31.9 148.7/155.5/3 3.8/5.2
  • The alloys of Table 8 were solution heat treated in a fluidized bed furnace 60 seconds at the temperature listed in Table 8. Subsequently the alloys were cold rolled 25% to 0.009″ then subjected to an aging anneal of 450 to 500° C. for 3 hours. After an additional cold reduction of 22% to 0.007″ samples were aged annealed at temperatures of 300 to 400° C. for 3 hours. Properties from samples given first and second ages at 450° C. and 300° C., respectively, are listed in Table 10. The Co-only alloys displayed a sensitivity to overall alloying levels with this scheme which was not found in alloys containing Cr. The only Co-only alloys at 150 ksi yield strength and above were K077 and K078, while all Cr-containing alloys reached or came close to that strength level. Strength-bend properties for this process are fairly similar to those in Table 9.
  • TABLE 10
    Properties from SA-CR-age-CR-age process of Example 5
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    K077 450/300 29.1 152.8/160.2/2 3.7/4.3
    K078 450/300 30.1 149.7/157.7/4 4.0/4.9
    K079 450/300 35.2 133.4/140.3/2
    K080 450/300 32.2 133.1/139.6/2
    K081 450/300 32.2 133.0/138.8/2
    K082 450/300 44.9 100.7/112.9/3
    K083 450/300 30.2 140.7/145.8/3
    K084 450/300 31.8 141.7/146.7/3 4.0/5.1
    K085 450/300 31.2 141.4/146.7/2
    K086 450/300 30.3 150.8/156.6/2 4.9/6.7
    K087 450/300 30.2 153.4/158.7/2 4.6/4.9
    K088 450/300 28.6 153.7/159.4/2 3.7/6.7
    K089 450/300 29.8 148.9/155.4/1 4.6/6.7
    K090 450/300 29.9 151.3/155.9/3 4.6/4.3
    K091 450/300 30.0 152.4/159.5/1 4.0/6.7
    K092 450/300 32.5 149.6/156.4/3 4.3/6.7
    K093 450/300 30.3 147.1/152.7/2 4.6/6.7
    K094 450/300 29.9 150.4/156.9/2 4.3/4.9
    K095 450/300 30.0 155.9/165.3/2 4.0/6.7
    K096 450/300 31.8 157.5/165.4/3 4.0/6.7
    K097 450/300 32.0 155.1/161.6/3 4.3/4.9
  • Example 6 Nickel:Cobalt Ratio
  • Laboratory ingots with the compositions listed in Table 11 were melted in a graphite crucible and Tamman cast into steel molds, which after gating were 4.33″×2.17″×1.02″. FIG. 11 is a flow chart of the process of this Example 6. For a target Si-content of 1% and Cr-content of 0.5% one alloy is Co-containing and the other is Co-free, the Ni-content is adjusted in order to keep a stoichiometric ratio ((Ni+Co)/(Si−Cr/5)) of close to 4.2. After soaking two hours at 900° C. they were hot rolled to 0.472″, thereby reheated after each pass at 900° C. for 10 minutes. After the last pass the bar was water quenched. After trimming and milling to 0.394″ in order to remove the surface oxide, the alloys were cold rolled to 0.0106″ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 11. Time and temperature were selected to achieve grain sizes below 20 μm. The alloys were then subjected to an aging anneal of 450 to 500° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.0079″ and aged at 300 or 400° C. for 3 hours. Properties measured after the second age anneal are presented in Table 12. The formability was measured via V-block. The data indicates that both alloys are capable of achieving a yield strength of 135 ksi, yet the Co-containing variant BS shows a better softening resistance that can be seen with increasing the age annealing temperature. The slightly better bad way bendability of variant BS is presumably due to the slightly lower grain size after solution annealing.
  • TABLE 11
    Alloys of Example 6, wt. %
    (Ni + Co)/(Si − Grain
    alloy Ni Co Cr Si Mg Cr/5) Ratio* Ni/Co SA conditions size, μm
    BR 3.59 0.48 1.00 3.97 915° C. - 1 10-15
    minute
    BS 3.18 0.47 0.49 0.97 4.19 6.77 950° C. - 1  5-10
    minute
  • TABLE 12
    Properties from SA-age-CR-age Process of Example 6
    1.AA 2.AA 300° C./3 h 2AA 400° C./3 h
    Temp 90° 90°
    Alloy ° C. YS ksi TS ksi A10% % IACS MINBR/ YS ksi TS ksi A10% % IACS MINBR/
    BR 450 135.8 144.2 3.7 32.5 4.0/5.0 118.2 129.5 6.5 37.1 —/—
    475 133.9 141.8 3.7 35.1 4.0/6.0 124.0 132.9 7.9 38.5 —/—
    500 117.3 123.6 5 37.1 4.0/4.0 100.1 108.8 11 41.6 —/—
    BS 450 135.8 142.6 1.8 31.7 4.0/4.0 128.2 137.2 3.7 33.5 3.5/4.0
    475 132.7 138.4 1.7 34.6 5.0/5.5 126.5 136.2 2.3 38.3 4.0/4.5
    500 127.3 134.7 4.8 37.4 4.0/5.0 119.4 127.8 6 41.2 —/—
  • Example 7 (Ni+Co)/(Si−Cr/5) Ratio
  • A group of alloys was cast and processed using once more the basic compositions of K068 (Co only), K070 (Co and Cr) and K072 (Cr only) from Table 5 as a base, but in this case with a gradual drop in Si levels, thus increasing the (Ni+Co)/(Si−Cr/5) stoichiometric ratio above the 3.6 to 4.2 range of previous alloys. Ni and Co levels were designed to be constant for each of the three alloy types. A series of ten pound laboratory ingots with the compositions listed in Table 11 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. K143 to K146 are variants of K072, K160 to K163 variants of K070, and K164 to K167 are variants of K068. FIG. 12 is a flow chart of the process of this Example 7. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1″ (1.6″/1.35″/1.1″), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench. The quenched plates were then soaked at 5900° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling. The alloys were then cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for 60 seconds at the temperatures listed in Table 13. The temperature was selected to maintain a fairly constant grain size. The alloys were then cold rolled 25% to 0.009″ and aged 450, 475 and 500° C. for 3 hours. Properties after each aging temperature for alloys of the current example, as well as K068, K070, K072, K078, K087 and K089 are listed in Table 14. For each alloy type, yield strength decreases as the stoichiometric ratio increases above about 4.5, and fails below 120 ksi at a ratio of around 5.5. This is shown in FIGS. 13 to 15 for the Cr alloys (plus K072 data), the Co-alloys (plus K068 and K078 data), and the Co—Cr alloys (plus K070, K087 and K089 data), respectively. In the Co and Cr alloys, conductivity decreases as the stoichiometric ratio increases above about 4.5, while for the alloys with both Co and Cr there is not a clear relationship between stoichiometry and conductivity. This is shown graphically in FIGS. 16 through 18. Based on this data it is evident that the best yield strength-conductivity properties are produced when the stoichiometric ratio is kept between 3.5 and 5.0.
  • TABLE 13
    Alloys of Example 7
    (Ni +
    Co)/
    (Si −
    Cr/5) SA
    alloy Ni Co Cr Si Mg Ratio Ni/Co Temperature
    K143 4.61 0.519 1.11 0.099 4.582 950
    K144 4.63 0.503 0.828 0.074 6.365 950
    K145 4.59 0.607 0.91 0.085 5.820 950
    K146 4.55 0.576 0.803 0.093 6.615 950
    K160 3.84 1.2 0.52 1.19 4.641 3.20 975
    K161 3.8 1.18 0.515 1.1 4.995 3.22 975
    K162 3.83 1.2 0.513 1.03 5.424 3.19 975
    K163 3.84 1.21 0.556 0.938 6.108 3.17 975
    K164 3.74 1.17 1.05 0.104 4.676 3.20 975
    K165 3.9 1.23 1.01 0.116 5.079 3.17 975
    K166 3.87 1.23 0.918 0.12 5.556 3.15 975
    K167 3.9 1.24 0.83 0.085 6.193 3.15 975
  • TABLE 14
    Properties after solution annealing, cold rolling 25% and aging of Example 7
    450° C. age 475° C. age 500° C. age
    alloy YS, ksi % IACS 90° bends YS, ksi % IACS 90° bends YS, ksi % IACS 90° bends
    K143 138.9 31.2 2.9/2.0 135.8 33.7 2.0/2.7 126.3 35.8 2.0/2.2
    K144 118.1 27.5 1.8/2.2 125.6 30.8 1.3/1.1 121.3 33.1 2.2/1.3
    K145 120.8 27.3 2.0/1.3 127.5 30.3 2.2/1.3 123.5 32.6 2.2/1.8
    K146 113.4 26.8 1.8/1.1 121.7 30.4 2.2/2.0 116.8 32.2 1.3/1.6
    K160 127.4 29.5 2.0/3.1 133.8 34.0 2.4/1.6 122.6 39.3 1.8/1.8
    K161 127.4 29.4 2.4/1.1 131.3 33.0 2.2/1.6 123.5 35.7 1.8/0.7
    K162 122.4 33.4 1.3/1.3 120.7 34.4 2.4/1.3 116.5 35.9 1.6/1.3
    K163 120.7 29.8 1.3/1.1 119.4 32.0 1.6/1.1 111.1 34.2 1.6/1.1
    K164 126.6 29.9 2.4/1.6 132.6 33.7 2.4/2.0 125.8 36.7 2.0/2.9
    K165 118.9 29.6 2.2/1.6 124.0 32.9 2.2/2.4 119.5 35.4 1.6/1.8
    K166 116.6 27.9 2.0/1.3 120.4 30.4 2.9/1.1 117.7 32.5 2.0/1.8
    K167 111.6 25.7 2.0/1.6 114.5 27.4 1.6/1.3 113.4 29.3 1.3/0.2
    K068 131.9 29.3 2.2/2.8 131.7 33.5 2.2/2.2
    K070 134.7 29.7 2.2/1.6 129.7 33.6 1.7/1.6
    K072 133.3 29.9 1.7/1.7 130.0 33.2 1.6/2.2
    K078 125.3 30.8 133.3 31.9 2.2/1.6 125.7 36.3
    K087 133.4 29.0 136.9 30.7 2.2/1.6 124.1 37.7
    K089 136.2 29.9 135.0 30.6 131.5 34.4
  • Example 8 (Ni+Co)/(Si−Cr/5) Ratio
  • A series of ten pound laboratory ingots with the compositions listed in Table 15 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. FIG. 19 is a flow chart of the process of this Example 8. After soaking two hours at 900° C. they were hot rolled in three passes to 1.1″ (1.6″/1.35″/1.1″), reheated at 900° C. for 10 minutes, and further hot rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench. The quenched plates were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling. The alloys were then cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C. Grain size ranged from 6 to 12 μm. Alloys were then subjected to an aging anneal of 450 or 475° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009″ and aged at 300° C. for 4 hours. Properties measured after the second age anneal are presented in Table 16.
  • Table 17 has properties measured after samples were solution heat treated in a fluidized bed furnace for 60 seconds at 950° C., cold rolled 25% to 0.009″, given an aging anneal at 475° C. for 3 hours, cold rolled 22% to 0.007″, and given a final anneal of 300° C. for 3 hours. The results show the viability of a range of compositions with Si from 1.0 to 1.2%, with a Ni/Co ratio of 4, and a stoichiometric ratio (((Ni+Co)/(Si−Cr/5))) of 3.5 to 5.0. This is shown graphically in FIGS. 20 and 21, which plot conductivity and yield strength data from Table 17 versus the stoichiometric ratio. These plots show yield strengths of 140 ksi or higher combined with conductivities of 25% IACS or higher are obtained for this process when the ratio is between 3.0 and 5.0. Cr was not found to influence properties significantly in the alloys of this example.
  • Stress relaxation tests were run on samples of K188 and K205 which were cold rolled to 0.012″ from milled hot rolled plate, solution annealed at 950° C. for 60 seconds, cold rolled 25% to 0.009″, and age annealed at 475° C. for 3 hours. The stress relaxation tests were run at 150° C. for 3000 hours on samples of longitudinal and transverse orientation. Results in Table 18 show that both alloys had excellent stress relaxation resistance, over 85% stress remaining after 1000 hours at 150° C., regardless of Cr content or sample orientation.
  • TABLE 15
    Alloys of Example 8
    Alloy Analyzed composition, wt % Ni/Co Stoichiometric ratio Grain Size, μm
    K188 Cu—3.40Ni—0.81Co—1.16Si—0.42Cr—0.019Mg 4.20 3.91 7.3
    K189 Cu—3.20Ni—0.72Co—1.05Si—0.38Cr—0.033Mg 4.46 4.02 10.1
    K190 Cu—3.22Ni—0.70Co—1.28Si—0.31Cr—0.036Mg 4.59 3.22 8.5
    K191 Cu—3.22Ni—0.70Co—1.05Si—0.53Cr—0.064Mg 4.58 4.16 9.5
    K192 Cu—2.94Ni—0.69Co—1.29Si—0.55Cr—0.062Mg 4.24 3.08 10.9
    K193 Cu—3.21Ni—0.90Co—1.05Si—0.34Cr—0.117Mg 3.56 4.18 8.6
    K194 Cu—3.20Ni—0.84Co—1.30Si—0.22Cr—0.035Mg 3.80 3.22 7.8
    K195 Cu—3.18Ni—0.86Co—0.81Si—0.52Cr—0.070Mg 3.71 5.72 7.1
    K196 Cu—3.19Ni—0.89Co—1.28Si—0.57Cr—0.111Mg 3.60 3.49 7.7
    K197 Cu—3.61Ni—0.70Co—1.06Si—0.36Cr—0.067Mg 5.14 4.36 10.7
    K198 Cu—3.60Ni—0.70Co—1.28Si—0.39Cr—0.077Mg 5.13 3.58 8.7
    K199 Cu—3.60Ni—0.70Co—1.06Si—0.60Cr—0.076Mg 5.13 4.58 9.3
    K200 Cu—3.60Ni—0.70Co—1.28Si—0.60Cr—0.092Mg 5.14 3.70 9.3
    K201 Cu—3.63Ni—0.88Co—1.04Si—0.29Cr—0.065Mg 4.12 4.59 6.0
    K202 Cu—3.62Ni—0.90Co—1.27Si—0.36Cr—0.101Mg 4.04 3.77 7.4
    K203 Cu—3.59Ni—0.89Co—1.05Si—0.56Cr—0.076Mg 4.04 4.77 6.1
    K204 Cu—3.58Ni—0.88Co—1.27Si—0.56Cr—0.075Mg 4.09 3.85 5.9
    K205 Cu—3.73Ni—0.91Co—1.13Si—0.082Mg 4.09 4.11 12.1
    K206 Cu—3.53Ni—0.81Co—1.02Si—0.080Mg 4.36 4.25 12.2
    K207 Cu—3.53Ni—0.78Co—1.25Si—0.055Mg 4.55 3.44 9.9
    K208 Cu—3.57Ni—1.00Co—1.02Si—0.070Mg 3.57 4.48 7.6
    K209 Cu—3.54Ni—1.02Co—1.25Si—0.085Mg 3.47 3.65 7.4
    K210 Cu—3.94Ni—0.82Co—1.06Si—0.149Mg 4.78 4.49 9.5
    K211 Cu—3.97Ni—0.80Co—1.24Si—0.065Mg 4.97 3.85 11.5
    K212 Cu—3.95Ni—0.99Co—1.04Si—0.100Mg 4.01 4.75 10.2
    K213 Cu—3.97Ni—0.99Co—1.22Si—0.079Mg 4.01 4.07 10.2
  • TABLE 16
    SA-age-CR-age process properties of Example 8
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    K188 450/300 29.3 149.5/156.1/2 3.3/5.2
    K189 475/300 33.6 147.3/153.8/2 4.0/4.0
    K204 450/300 29.7 149.6/155.1/2 4.0/5.2
    K205 475/300 34.2 149.8/155.7/2 4.0/5.2
    K206 475/300 35.0 147.9/153.9/2 4.0/5.3
    K213 475/300 34.2 150.8/157.4/2 5.2/5.2
  • TABLE 17
    SA-CR-age-CR-age process properties of Example 8
    YS/TS/EI
    Alloy Ages % IACS ksi/ksi/% 90° MBR/t
    K188 475/300 35.1 145.7/152.4/3 2.0/4.9
    K189 475/300 34.7 146.1/152.6/2 2.6/5.7
    K190 475/300 28.0 139.2/148.5/4 2.9/5.1
    K191 475/300 37.2 143.7/149.9/3 3.4/6.7
    K192 475/300 28.1 139.7/146.4/2 2.6/6.7
    K193 475/300 36.2 143.6/149.3/3 2.9/5.1
    K194 475/300 29.1 138.7/146.1/3 2.6/6.7
    K195 475/300 35.5 130.7/134.7/4 2.0/3.4
    K196 475/300 30.2 143.4/149.5/2 2.6/9.0
    K197 475/300 35.4 145.3/152.0/2 3.1/6.7
    K198 475/300 31.7 148.2/155.7/3 2.9/6.7
    K199 475/300 35.5 147.8/154.4/3 2.9/9.0
    K200 475/300 33.7 146.3/152.9/3 3.4/6.7
    K201 475/300 36.8 145.2/150.0/2 2.9/6.7
    K202 475/300 33.5 146.1/152.8/3 2.6/5.1
    K203 475/300 34.4 147.4/153.6/2 3.6/5.7
    K204 475/300 33.9 150.3/156.8/3 2.9/6.7
    K205 475/300 35.3 147.0/152.8/2 2.9/5.7
    K206 475/300 35.8 146.9/153.7/3 2.4/6.7
    K207 475/300 29.7 143.3/150.3/2 2.6/6.7
    K208 475/300 36.2 142.5/148.1/3 2.9/6.7
    K209 475/300 32.2 145.5/152.1/3 2.6/6.7
    K210 475/300 34.1 148.6/154.1/5 2.9/6.7
    K211 475/300 33.8 144.7/152.1/2 3.1/5.1
    K212 475/300 34.5 140.6/145.4/3 2.9/5.7
    K213 475/300 35.0 148.4/154.4/2 3.6/6.7
  • TABLE 18
    150° C. Stress Relaxation Data for samples cold rolled
    25% and aged at 475° C. for 3 hours of Example 8
    Longitudinal Transverse
    (in percent (in percent
    Yield Strength, stress remaining) stress remaining)
    Alloy ksi 1000 hr 3000 hr 1000 hr 3000 hr
    K188 (Cr) 136.4 89.9 87.9 88.2 85.2
    K205 (no Cr) 132.2 92.0 90.4 91.6 89.6
  • Example 9 Effect of Cr
  • A series of ten pound laboratory ingots with the compositions listed in Table 19 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. FIG. 22 is a flow chart of the process of this Example 9. The ingots were then machined to have tapered edges, as illustrated schematically in FIG. 23, to create a higher state of tensile stress at the edges. This condition is more prone to edge cracking than the standard flat edges, and thus more sensitive to alloying additions, in this case Cr. The alloys were soaked for two hours at 900° C., and rolled in two passes to 1.12″ (1.4″/1.12″) then water quenched. After examination for cracks, the bars were reheated at 900° C. for two hours, and rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench. It was found that without Cr, K224 developed large cracks during the first few passes of hot rolling, which enlarged during the remaining passes. None of the Cr-containing alloys developed large cracks during hot rolling. A few of the alloys showed small cracks after initial passes believed to be due to casting defects, but these did not enlarge during subsequent passes. The Cr effect was the same independent of Cr level, from 0.11% to 0.55%. Examples of edge conditions of K224 and K225 after hot rolling are shown in FIGS. 24 and 25. The addition of even a small amount of Cr would reduce cracking in plant production, thus improving yield after hot rolling and coil milling Data from plant-cast bars (i.e., bars cast as pilot product dc castings), whose compositions are listed in Table 20, show the beneficial effect of Cr on preventing hot rolling cracks and therefore improving yield. Table 21 lists the normalized casting plant yield (CPY) of six Cr-containing and four non-Cr bars, where the normalized CPY is obtained as follows: First the individualized CPY is calculated as the ratio of coil milled weight to cast bar weight. Second the bar with the highest CPY, in this case RN 033410, is assigned a normalized CPY of 100%. Third the normalized CPY of all other bars is calculated by dividing the CPY of each bar by the CPY of RN033410. The normalized CPY of bars without Cr is 48-82% compares to 82-100% for the Cr-containing bars
  • Limiting the Cr level would be desirable due to the abrasiveness of Cr-silicides, which is demonstrated in FIG. 26. FIG. 26A shows wear on a tool steel ball which was slid for 3000 linear inches (1500 inches on each side of the strip) under a 100 gm load over the strip surface with lard oil as a lubricant of a non-Cr sample (RN033407) that was plant solution annealed at 975° C., cold rolled 25% then aged a 450° C. and sulfuric acid cleaned, while FIG. 26B has a similar condition using a sample of a Cr-containing alloy (RN834062). The polished appearance of the ball shown in FIG. 26 shows that the Cr-containing alloy caused much more wear, leading to a significantly larger volume of material being removed from the ball. This is seen in FIG. 26 as a much larger wear scar for the Cr-containing alloy. The larger wear scar suggests that during stamping of a sheet of the alloy into parts, a high amount of tool wear would occur.
  • TABLE 19
    Alloys used in Example 9
    Alloy Ni Co Cr Si Mg
    K224 3.71 0.91 0 1.14
    K225 3.71 0.93 0.11 1.19 0.030
    K226 3.61 0.82 0.23 1.20 0.035
    K227 3.50 0.95 0.34 1.20 0.035
    K228 3.51 0.85 0.46 1.21 0.040
    K229 3.39 0.85 0.55 1.20 0.043
  • TABLE 20
    Compositions of plant-cast bars of Example 91
    Bar Ni Co Cr Si Mg
    RN032037 3.71 0.75 1.09 0.12
    RN032038
    RN033407 3.66 0.88 1.07 0.106
    RN033408
    RN033409 3.83 0.89 0.45 1.22 0.138
    RN033410
    RN834059 3.24 0.758 0.425 1.02 0.094
    RN834060
    RN834061 3.45 0.74 0.44 1.14 0.076
    RN834062
  • TABLE 21
    Milling data for plant-cast bars of
    Example 9
    CPY %
    Bar Type (NORMALIZED)
    RN032037 Non Cr 75.2%
    RN032038 Non Cr 48.1%
    RN033407 Non Cr 76.0%
    RN033408 Non Cr 82.3%
    RN033409 Cr 95.6%
    RN033410 Cr
     100%
    RN834059 Cr 92.1%
    RN834060 Cr 90.1%
    RN834061 Cr 87.7%
    RN834062 Cr 82.0%
  • A single casting run produced three bars with the composition shown in Table 21a. Casting plant yield of the bars, which was normalized similarly to the data of Table 21 where RN033410 is considered 100%, is given in Table 21b. The CPY of the low-Cr bars compares favorably with the Cr-containing bars of Table 21. This is believed to be due to Cr reducing cracking during hot rolling even at these low levels. RN037969 has a normalized CPY % above 100 due to the fact that the yield of this bar was higher than RN033410 in the earlier example.
  • TABLE 21a
    Analyzed compositions of low-Cr bars cast and processed in the plant
    Bar Ni Co Cr Si Mg
    037969 3.70 0.98 0.059 1.07 0.093
    037970
    037971
  • TABLE 21b
    CPY %
    Bar Type (normalized)
    RN037969 Low-Cr 102.1% 
    RN037970 Low-Cr 89.8%
    RN037971 Low-Cr 68.4%
  • Example 10 Effect of Cr, Mn
  • A series of ten pound laboratory ingots with the compositions listed in Table 22 were melted in a silica crucible and Durville cast into steel molds, which after gating were approximately 4″×4″×1.75″. FIG. 27 is a flow chart of the process of this Example 10. Alloy K259 contains a smaller level of Cr than those alloys in Example 9, to investigate the lower limits of the beneficial effect of Cr on hot rolling. Alloys K251, K254 and K260 contain low levels of Mn, to determine if Mn affects hot reliability in the alloy of this invention. The ingots were then machined to have tapered edges, as illustrated schematically in FIG. 23, to create a higher state of tensile stress at the edges. The alloys were soaked for two hours at 900° C., and rolled in two passes to 1.12″ (1.4″/1.12″) then water quenched. After examination for cracks, the bars were reheated at 900° C. for two hours, and rolled in three passes to 0.50″ (0.9″/0.7″/0.5″), followed by a water quench. K259, with 0.058% Cr, hot rolled without edge crack formation. The Mn-containing alloys, along with K261 (with neither Cr nor Mn) developed large edge cracks. Thus a Cr addition near 0.05%, with a preferred range of 0.025 to 0.1% Cr, appears to be appropriate to balance hot rollability and formation of abrasive particles that would lead to tool wear.
  • The quenched bars were then soaked at 590° C. for 6 hours, trimmed and then milled to remove surface oxides developed during hot rolling. The alloys were then cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C. Alloys were then subjected to an aging anneal of 475° C. for 3 hours, designed to increase strength and conductivity. The alloys were then cold rolled 25% to 0.009″ and aged at 300° C. for 3 hours. Alternatively, after solution heat treatment the alloys were cold rolled 25% to 0.009″, given an aging anneal at 475° C. for 3 hours, cold rolled 22% to 0.007″, and given a final anneal of 300° C. for 3 hours. Properties after the final age for both process paths are listed in Table 23. For both processes, the exceptionally good property combination of 150 ksi yield strength and at least 31% IACS are achieved, with low levels of Cr, Mn or neither. Conductivity and yield strength are plotted in FIGS. 28 and 29 against the stoichiometric ratio ((Ni+Co)/(Si−Cr/5)) along with data from example 8 to demonstrate the unusually good properties reached when the ratio is kept between 3.0 and 5.0.
  • TABLE 22
    Low Cr and Mn alloys of Example 10
    Alloy Ni Co Si Mg Cr Mn Ratio*
    K251 3.64 0.84 1.16 0.058 0.026 3.862
    K254 3.73 0.90 1.16 0.044 0.061 3.991
    K259 3.78 0.56 1.14 0.073 0.058 0.004 3.846
    K260 3.75 0.94 1.15 0.065 <.001 0.048 4.078
    K261 3.79 0.95 1.16 0.054 <.001 0.004 4.086
    *Ratio = (Ni + Co)/(Si − Cr/5)
  • TABLE 23
    Properties for Example 10
    SA-age-CR-age process SA-CR-age-CR-age process
    % 90° % 90°
    Alloy IACS YS/TS/EI MBR/t IACS YS/TS/EI MBR/t
    K251 31.0 149.9/156.5/1 4.0/5.2 32.0 151.9/158.6/3 2.6/2.9
    K254 33.7 141.2/144.7/2 3.3/3.3 33.0 151.7/158.1/1 2.3/3.7
    K259 31.8 151.0/157.3/2 4.0/5.2 33.3 150.8/156.9/2 2.3/2.9
    K260 32.4 149.9/156.3/3 3.8/3.8 35.3 148.6/154.7/3 2.9/4.3
    K261 31.9 150.9/157.1/2 3.8/5.2 34.4 151.0/157.6/2 2.6/4.3
  • Example 11 Effect of Processing
  • Sections of plant cast bar RN032037, whose composition is in Table 20, were processed from plant hot rolled and coil milled plate 0.600″ thick. Samples were further processed by a variety of processing paths shown in FIG. 30. Process A involved cold rolling to 0.012″ and solution heat treating in a fluidized bed furnace for 60 seconds at 950° C., age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009″, and giving a second anneal at 350° C. for 4 hours. In process B, the metal was rolled to 0.050″ and given an intermediate bell anneal (“IMBA”) of 575° C. for 8 hours. Then the samples were subject to cold rolling to 0.012″ and solution heat treating in a fluidized bed furnace for 60 seconds at 950° C., age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009″, and giving a second anneal at 350° C. for 4 hours, In process C, The alloy was rolled to 0.024″ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C., followed by cold rolling to 0.012″ and a second solution heat treatment in a fluidized bed furnace for 60 seconds at 950° C. Subsequently, the process involved age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009″, and giving a second anneal at 350° C. for 4 hours. In process D, cold rolling to 0.012″ was followed by solution heat treatment in a fluidized bed furnace for 60 seconds at 950° C. the alloy was cold rolled 25% to 0.009″, given an aging anneal at 475° C. for 3 hours, cold rolled 22% to 0.007″, and given a final anneal of 300° C. for 3 hours. In process E, the metal was rolled to 0.050″ and given an intermediate bell anneal of 575° C. for 8 hours. Then the samples were rolled to 0.024″ and solution heat treated in a fluidized bed furnace for 60 seconds at 950° C., followed by cold rolling to 0.012″ and a second solution heat treatment in a fluidized bed furnace for 60 seconds at 950° C. Subsequently, the process involved age annealing at 500° C. for 3 hours, cold rolling 25% to 0.009″, and giving a second anneal at 350° C. for 4 hours.
  • TABLE 24
    Properties resulting from the processes of Example 11
    Process Description YS/TS/EI % IACS 90° MBR/t
    A “Standard” process 145.1/152.7/3 36.2 4.0/7.0
    B IMBA process 144.4/150.4/3 37.4 3.8/4.0
    C Double solution anneal 147.2/152.7/3 37.1 3.6/6.9
    process
    D SA-CR-age-CR-age 146.5/154.4/2 34.2 4.2/8.7
    process
    E IMBA-double SA 143.6/150.1/3 36.7 3.3/7.0
    process
  • Example 12 Effect of Processing
  • Sections of plant cast bar RN032037, whose composition is in Table 20, were processed from plant hot rolled and coil milled plate 0.600″ thick. Process variables were systematically varied to explore a matrix containing ranges of processing conditions. FIG. 31 is a flow chart of the process of this Example 12. After cold rolling to 0.012″, samples were solution annealed in a fluidized bed furnace at temperatures of 925, 950, 975 and 1000° C. for 60 seconds. Coupons were then given age anneals at temperatures of 450, 475, 500 and 525° C. for three hours. Samples were then cold rolled to final thickness at varying reductions of 15, 25 and 35%. Finally, samples were given a second age anneal for four hours at 300, 325, 350 and 375° C. Table 25 contains properties of samples with different solution anneal temperatures while the rest of the process was held constant. As solution temperature is increased, yield strength increases, while conductivity decreases. Additionally, bend formability worsens at the higher solution annealing temperatures, due to the large grain size developed during the 975 and 1000° C. anneals. Thus a solution annealed grain size below 20 μm is preferred.
  • When the temperature of the first age is varied while the other processing variables are held constant, it is found that the highest strength levels are due to the intermediate aging temperatures, as shown for the 475 and 500° C. ages in Table 26. Also, the conductivity increased with increasing aging temperature. Thus the first age temperature can be manipulated to provide various desirable combinations of strength and conductivity.
  • When the roll reduction between the first and second ages was varied, yield strength was found to increase with increasing reduction, in this case up to 35%, while conductivity was unaffected. A larger increase in strength was found when going from 15 to 25% reduction than when going from 25 to 35%. Bend formability was found to worsen with higher reductions. The roll reduction can be manipulated to affect the strength-formability characteristics of the material produced. Use of roll reduction above 35% may be useful to produce peak strength, albeit with poorer formability.
  • Table 28 shows that the second age anneal temperature does not have a large effect on properties when the other processing variables are held constant. Conductivity was found to increase as the temperature of the second age increased, but to a small degree. Thus a wide operating range is acceptable for this step of the process.
  • TABLE 25
    Effect of varying solution anneal temperatures, with 475° C.
    first age, 25% roll reduction, 350° C. second age of Example 12
    SA temperature, SA grain size,
    ° C. μm YS/TS/EI % IACS 90° Bends
    925 9.0 142.3/147.7/3 36.0 6.0/6.0
    950 12.9 145.9/152.3/3 34.1 6.1/6.1
    975 26.1 146.5/152.6/2 32.3  6.1/12.1
    1000 28.8 147.5/152.1/3 32.7  8.7/12.1
  • TABLE 26
    Effect of varying first age temperatures, with 950° C. solution
    anneal, 25% roll reduction, 350° C. second age of Example 12
    1st Age Temp, ° C. YS/TS/EI % IACS 90° Bends
    450 140.1/145.2/4 30.5 4.0/6.1
    475 145.9/152.3/3 34.1 6.1/6.1
    500 145.1/152.7/3 36.2 4.0/7.0
    525 133.2/134.5/1 39.9 n/m*
    *not measured
  • TABLE 27
    Effect of varying roll reductions, with 950° C. solution
    anneal, 475° C. first age, 350° C. second age
    Roll reduction YS/TS/EI % IACS 90° Bends
    15% 138.4/145.0/4 33.9 5.4/5.4
    25% 145.9/152.3/3 34.1 6.1/6.1
    35% 148.9/155.5/3 34.0  7.1/10.0
  • TABLE 28
    Effect of varying second age temperatures, with 950° C.
    solution anneal, 475° C. first age, 25% roll reduction
    2nd Age Temp, ° C. YS/TS/EI % IACS 90° Bends
    300 146.4/152.0/2 33.2 6.1/6.1
    325 146.5/152.3/3 33.6 6.1/8.7
    350 145.9/152.3/3 34.1 6.1/6.1
    375 146.2/152.7/3 34.8 6.0/8.6
  • Samples from the Cr-free plant-cast bar RN033407 (composition in Table 20) were rolled in the laboratory from the coil milled condition at 0.460″ down to 0.012″. Subsequently samples were solution heat treated in a fluidized bed furnace for 60 seconds at 900° C. Coupons were then rolled 25% to 0.009″ and age annealed at 425, 450 and 475° C. for times of 4 and 8 hours at each temperature. Subsequently samples were cold rolled 22% to 0.007″ and given a final anneal of 300° C. for three hours. The best combination of strength and conductivity resulted from the 450° C. for 8 hour age, with the properties from that condition and others listed in Table 28a. Comparing the 450° C./8 hr data to the properties in Table 25, it is clear that further reducing the solution annealing temperature to 900° C. lowers the yield strength and increases conductivity to produce the unique combination of 140 ksi and 39% IACS. In addition, the processing including a 900° C. solution annealing temperature produced improved bend formability when compared to processing involving higher solution anneal temperatures.
  • TABLE 28A
    Properties after processing which includes a 900° C. solution anneal.
    1st age
    condition SA grain size, μm YS/TS/EI % IACS 90° Bends
    450° C./4 hr 5.5 138.5/143.0/2 36.1 2.6/4.0
    450° C./8 hr 5.5 140.3/144.7/2 39.0 2.0/4.3
    475° C./4 hr 5.5 126.9/131.7/3 40.7 2.3/4.0
    475° C./8 hr 5.5 131.0/135.0/3 41.2 1.7/2.3
  • Example 13 Effect of Si and Mg
  • Laboratory ingots with the compositions listed in Table 29 were melted in a graphite crucible and Tamman cast into steel molds, which after gating were 4.33″×2.17″×1.02″. All alloys were targeted to have a Cr-content of 0.5%. The Si-content was varied between 1.0% and 1.5%. For the high-Si 1.5% variants the Ni/Co ratio was varied between 4.98 and 11.37 with a fixed stoichiometric ratio ((Ni+Co)/(Si−Cr/5)) around 4. The influence of Mg was tested by alloy BW with the same alloy composition as BV but with additionally 0.1% Mg.
  • FIG. 32 is a flow chart of the process of this Example 13. After soaking two hours at 900° C. they were hot rolled to 0.472″, thereby reheated after each pass at 900° C. for 10 minutes. After the last pass the bar was water quenched. After trimming and milling to 0.394″ in order to remove the surface oxide, the alloys were cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 29. Time and temperature were selected to achieve grain sizes below 20 μm.
  • Subsequently the alloys were cold rolled 25% to 0.009″ then subjected to an aging anneal of 450 and 475° C. for 3 hours. Properties of samples are listed in Table 30. The formability was measured via V-block. With increasing Si-content the yield strength is increasing from 121 ksi for the 1.05% Si alloy to 135 ksi for the 1.51% Si alloy. For the 1.16% Si variants Mg results in a benefit to yield strength of 5-7 ksi. Lowering the Ni/Co ratio from 11.37 to 4.98 enhances yield strength for the high Si (1.5%) alloys. Stress relaxation was tested by the ring method with a target initial stress of 0.8 times yield strength. Table 31 shows the stress relaxation data for variants BV, BW and BX. Comparing BV and BW, due to Mg addition the stress relaxation resistance increases from 66.3% to 86.6% for the 150° C./1000 h condition and from 48.5% to 72.3% for the 200° C./1000 h condition. The stress relaxation resistance of the higher Si-containing BX amounts to 82.3% for the 150° C./1000 h condition and 68.7% for the 200° C./1000 h condition.
  • TABLE 29
    Alloys of Examples 13 and 15, wt %
    alloy Ni Co Cr Si Mg Ratio* Ni/Co SA conditions Grain size, μm
    BU 3.08 0.69 0.57 1.05 4.03 4.46 950° C. - 1 minute 10-15
    BV 3.51 0.75 0.49 1.16 4.01 4.68 950° C. - 1 minute 10-15
    BW 3.52 0.78 0.51 1.16 0.11 4.06 4.51 950° C. - 1 minute 15
    BT 4.04 1.15 0.47 1.41 3.94 3.51 975° C. - 1 minute  5
    BX 4.89 0.43 0.50 1.48 3.86 11.37 975° C. - 1 minute 15-20
    BY 4.48 0.90 0.51 1.51 3.82 4.98 975° C. - 1 minute 10
    *Ratio = (Ni + Co)/(Si − Cr/5)
  • TABLE 30
    Properties fro SA-Cr-AA Process of Example 13
    Alloy AA T, ° C. YS, ksi % IACS 90° MINBR/t
    BU 450 121.0 27.6 2.2/1.3
    BV 450 121.8 32.5 1.7/1.3
    475 120.5 34.8 n.m.
    BW 450 126.9 31.8 2.2/2.6
    475 127.6 34.4 n.m.
    BT 450 127.5 28.6 n.m.
    475 128.9 32.1 n.m.
    BX 450 129.5 29.1 2.6/2.6
    475 125.9 31.1 n.m.
    BY 450 135.2 30 2.2/2.2
    475 134.0 31.4 3.4/2.1
  • TABLE 31
    Stree Relaxation of Process SA-CR 25%-AA
    450° C./3 h of Example 13
    remaining stress (%)
    Alloy YS, ksi % IACS 150° C./1000 h 200° C./1000 h
    BV 121.8 32.5 66.3 48.5
    BW 126.9 31.8 86.6 72.3
    BX 129.5 29.1 82.3 68.7
  • Example 14 Effect of Si and Mg
  • FIG. 33 is a flow chart of the process of this Example 14. Specimens of Example 13 were subsequently cold rolled to 0.007″ with a cold reduction of 22%. Thereafter the samples were aged annealed at temperatures of 300° C. to 400° C. for 3 hours. Properties from samples given second ages at 300° C. are listed in Table 32. The formability was measured via V-block.
  • The highest yield strength was achieved with a first aging temperature of 450° C. With increasing Si-content the yield strength is increasing from 131 ksi for the Si 1.05% alloy to 147 ksi for the Si 1.51% alloy. For the Si 1.16% variants Mg results in a benefit to yield strength of 7-10 ksi. Lowering the Ni/Co ratio from 11.37 to 4.98 enhances yield strength for the high Si 1.5% alloys by 3 ksi. Stress relaxation was tested by the ring method with a target initial stress of 0.8 times yield strength. Table 33 shows the stress relaxation data for BV, BW and BX for the process SA-CR -1.AA 450° C.-CR -2.AA 300° C.
  • Comparing BV and BW, due to Mg addition the stress relaxation resistance increases from 72.6% to 85.6% for the 150° C./1000 h condition and from 55.8% to 69.3% for the 200° C./1000 h condition. The stress relaxation resistance of the higher Si-containing BX amounts to 81.1% for the 150° C./1000 h condition and 66.1% for the 200° C./1000 h condition.
  • TABLE 32
    Properties from SA-CR-1AA-CR-2AA Process of Example 14
    2.AA 300° C./3 h
    YS,
    Alloy 1.AA T, ° C. ksi TS, ksi A10, % % IACS 90° MINBR/t
    BU 450 130.7 138.1 2.6 33.6 5.5/5.5
    BV 450 137.4 144.5 3.7 31.4 2.8/5.6
    475 130.8 137.8 4.8 34.8 2.8/5.0
    BW 450 144.0 143.6 2.3 32.1 3.3/7.8
    475 141.3 147.1 3.8 34 2.8/6.7
    BT 450 144.6 152.4 2.9 29.8 4.0/8.0
    475 137.8 146.2 4.2 34.1 4.0/7.0
    BX 450 143.7 155.2 2.8 28.6 3.3/7.8
    475 134.4 148.2 2.8 31.2 2.8/6.7
    BY 450 146.6 155.8 3 29.6 3.3/6.7
    475 137.8 150.0 4.3 32.2 3.3/6.7
  • TABLE 33
    Stress Relaxation Process SA-CR-1AA450° C.-CR-2AA300° C.
    of Example 14
    remaining stress (%)
    Alloy YS, ksi % IACS 150° C./1000 h 200° C./1000 h
    BV 137.4 31.4 72.6 55.8
    BW 144.0 32.1 85.6 69.3
    BX 143.7 28.6 81.1 66.1
  • Example 15 Effect of Si and Mg
  • Laboratory ingots with the compositions listed in Table 34 were melted in a graphite crucible and Tamman cast into steel molds, which after gating were 4.33″×2.17″×1.02″. The alloys were Cr-free and with a stoichiometric ratio ((Ni+Co)/(Si−Cr/5)) around 4.2. The Ni/Co ratio was about 4.5. Two alloys have a targeted Si-content of 1.1%, but varying Mg-content and one alloy has an Si-content of 1.4% and additionally Mg. FIG. 34 is a flow chart of the process of this Example 15. After soaking two hours at 900° C. they were hot rolled to 0.472″, thereby reheated after each pass at 900° C. for 10 minutes. After the last pass the bar was water quenched. After trimming and milling to 0.394″ in order to remove the surface oxide, the alloys were cold rolled to 0.012″ and solution heat treated in a fluidized bed furnace for the time and temperature listed in Table 34. Time and temperature were selected to achieve grain sizes below 20 μm.
  • Subsequently the alloys were cold rolled 25% to 0.009″ then subjected to an aging anneal of 450 and 475° C. for 3 hours. Properties of samples are listed in Table 35. The yield strength, formability measured with V-block and conductivity of the Cr-free FL and FM are similar to the Cr-containing BV and BW from Example 13, with comparable Si-content of 1.1%, Ni/Co ratio and stoichiometric ratio. As in Example 13, an addition of 0.1% Mg results in a benefit to yield strength of 7-8 ksi.
  • With increasing Si-content from 1.17% to 1.39% the yield strength is increasing from 126.6 to 130.5 ksi at the same solution annealing temperature. For variant FN, increasing the solution annealing temperature from 950° C. to 1000° C. results in an increase of yield strength of 10 ksi.
  • Stress relaxation was tested by the ring method with a target initial stress of 0.8 times yield strength. Table 36 shows the stress relaxation data for the processes with a solution annealing temperature of 950° C. Compared to the Cr-containing 1.16% Si samples of Example 13, BV and BW, the stress relaxation of FL and FM is slightly lower. Similar to Example 13, a Mg addition of 0.1% results in a stress relaxation increase from 64.6% to 82.7% for the 150° C./1000 h condition and from 44.3% to 69.2% for the 200° C./1000 h condition. The stress relaxation resistance of the Mg-containing, Si 1.39% variant FN amounts to 84.1% for the 150° C./1000 h condition and 65.9% for the 200° C./1000 h condition.
  • TABLE 34
    Alloys at Examples 15 and 16, wt. %
    alloy Ni Co Cr Si Mg Ratio* Ni/Co SA conditions Grain size, μm
    FL 3.71 0.90 1.09 4.23 4.12  950° C. - 1 minute 10
    FM 3.89 0.87 1.17 0.10 4.05 4.47  950° C. - 1 minute  5-10
    FN 5.19 0.99 1.39 0.10 4.47 4.90  950° C. - 1 minute 10
    1000° C. - 1 minute 15-20
    *Ratio = (Ni + Co)/(Si − Cr/5)
  • TABLE 35
    Properties from SA-CR-AA Process of Example 15
    AA T, 90° MINBR/t
    Alloy SA-conditions ° C. YS, ksi % IACS GW/BW
    FL  950° C. - 1 minute 450 118.6 29.5 2.6/1.3
    475 119.4 34.5 3.0/1.7
    FM  950° C. - 1 minute 450 126.6 30.2 2.6/2.2
    475 126 33.1 2.1/2.1
    FN  950° C. - 1 minute 450 130.5 30.7 3.0/2.6
    475 129.1 33.1 2.6/2.2
    1000° C. - 1 minute 450 141.7 27.1 3.5/3.9
    475 139.2 29.6 3.5/4.8
  • TABLE 36
    Stress Relaxation of Process SA 950° C.-CR 25%-
    AA 450° C./3 h of Example 15
    remaining stress (%)
    Alloy YS, ksi % IACS 150° C./1000 h 200° C./1000 h
    FL 118.6 29.5 64.6 44.3
    FM 126.6 30.2 82.7 69.2
    FN 130.5 30.7 84.1 65.9
  • Example 16 Effect of Si and Mg
  • FIG. 35 is a flow chart of the process of this Example 16. Specimens of Example 15 were subsequently cold rolled to 0.007″ with a cold reduction of 22%. Thereafter the samples were aged annealed at temperatures of 300° C. to 350° C. for 3 hours. Properties from samples given second ages at 300° C. are listed in Table 37. The formability was measured via V-block. The highest yield strength was achieved with a first aging temperature of 450° C.
  • FM shows a higher yield strength of 11 ksi in comparison to FL, that is partly ascribed to the Mg-content and partly ascribed to the slightly higher Si-content. The yield strength, bendability and conductivity of the Cr-free FL and FM are similar to the Cr-containing BV and BW from example 15, with comparable Si-content, Ni/Co ratio and stoichiometric ratio.
  • Increasing Si-content from 1.17% to 1.39% leads to the same yield strength of about 144 ksi for a solution annealing temperature of 950° C. For variant FN, increasing the solution annealing temperature from 950° C. to 1000° C. results in an increase of yield strength from 143 to 158 ksi.
  • Stress relaxation was tested by the ring method with a target initial stress of 0.8 times yield strength. Table 38 shows the stress relaxation data for FL and FM for the process SA 950° C.-CR-1.AA 450° C.-CR -2.AA 300° C. Compared to the Cr-containing 1.16% Si samples of example 15, BV and BW, the stress relaxation of FL and FM is lower by 2-3%. Similar to example 15, a Mg addition of 0.1% results in a stress relaxation increase from 70.0% to 82.0% for the 150° C./1000 h condition and from 52.3% to 66.9% for the 200° C./1000 h condition. The stress relaxation resistance of the Mg-containing, Si 1.39% variant FN amounts to 85.0% for the 150° C./1000 h condition and 66.4% for the 200° C./1000 h condition.
  • TABLE 37
    Properties from SA-CR-1AA-CR-2AA Process of Example 16
    2.AA 300° C./3 h
    Alloy SA-conditions 1.AA T, ° C. YS, ksi TS, ksi A10, % % IACS 90° MINBR/t GW/BW
    FL  950° C. - 1 minute 450 133.1 140 2.7 31.6 4.5/6.1
    475 129.7 139.5 1.9 36.2 3.9/4.4
    FM  950° C. - 1 minute 450 144 147.6 2 31 4.4/7.2
    475 141.3 145 1.8 33.2 4.5/6.8
    FN  950° C. - 1 minute 450 143.2 150.0 2 31.5 3.9/7.2
    475 133.1 138.9 2.4 34.3 3.3/5.6
    1000° C. - 1 minute 450 158.1 165.1 1.4 27.6 5.0/9.4
    475 157.5 164.6 1.9 30.9 4.4/8.3
  • TABLE 38
    Stress Relaxation of Process SA 950° C.-CR-1AA
    450° C.-CR-2AA 300° C. of
    remaining stress (%)
    Alloy YS, ksi % IACS 150° C./1000 h 200° C./1000 h
    FL 133.1 31.6 70.1 52.3
    FM 144.0 31 82.0 66.9
    FN 143.2 31.6 85.0 66.4
  • Example 16
  • FIG. 36 shows the relation between 90°-minBR/t BW and yield strength for the alloys and processes of Examples 13, 14, 15, and 16. Both processes SA-CR-AA and SA-CR-AA-CR-AA form two groups with a certain formability-yield strength relation. The solid lines are just a guide to the eye and mark increasing Min BR/t and increasing yield strength with higher Si-content and/or Mg-addition. There is almost no difference in yield strength and formability-yield strength relationship between the Cr-containing and Cr-free variants.
  • FIG. 37 shows the relation between % IACS and yield strength for the alloys and processes of Examples 13, 14, 15, and 16. The Cr-free and the Cr-containing alloys show the same capability in achieving a conductivity of 30% IACS together with high yield strength. The SA-CR-AA-CR-AA process achieves higher yield strength than the SA-CR-AA process, but at the same conductivity.

Claims (31)

1. A copper base alloy having an improved combination of yield strength and electrical conductivity consisting essentially of:
between about 1.0 and about 6.0 weight percent Ni;
up to about 3.0 weight percent Co;
between about 0.5 and about 2.0 weight percent Si;
between about 0.01 and about 0.5 weight percent Mg;
up to about 1.0 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities, the alloy processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 25% IACS.
2. The alloy according to claim 1 wherein the alloy has a conductivity of at least about 30% IACS.
3. The alloy according to claim 1 wherein the alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 38% IACS.
4. The alloy according to claim 1 wherein the alloy is processed to have a yield strength of at least about 143 ksi , and an electrical conductivity of at least about 37% IACS.
5. The alloy according to claim 1 wherein the alloy is processed to have a yield strength of at least about 157 ksi, and an electrical conductivity of at least about 32% IACS.
6. A copper base alloy having an improved combination of yield strength and formability consisting essentially of:
between about 1.0 and about 6.0 weight percent Ni;
up to about 3.0 weight percent Co;
between about 0.5 and about 2.0 weight percent Si;
between about 0.01 and about 0.5 weight percent Mg;
up to about 1.0 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities, the alloy processed to have a yield strength of at least about 137 ksi, and an mbr/t of less than 4 t for both good way bends and bad way bends.
7. The copper base alloy according to claim 6 wherein the alloy has an mbr/t of less than about 2 t for both good way bends and bad way bends.
8. The copper base alloy according to claim 6 wherein the alloy has an electrical conductivity of at least about 25% IACS.
9. The copper base alloy according to claim 8 wherein the alloy has an electrical conductivity of at least about 30% IACS.
10. A copper base alloy having an improved combination of yield strength, electrical conductivity, and formability, consisting essentially of:
between about 1.0 and about 6.0 weight percent Ni;
up to about 3.0 weight percent Co;
between about 0.5 and about 2.0 weight percent Si;
between about 0.01 and about 0.5 weight percent Mg;
up to about 1.0 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities, the ratio of (Ni+Co)/(Si−Cr/5) being between about 3 and about 7.
11. The alloy according to claim 10 wherein the alloy is processed to have an mbr/t of less than about 4 t for both good way bends and bad way bends.
12. The alloy according to claim 10 wherein the alloy is processed to have an mbr/t of less than about 2 t for both good way bends and bad way bends.
13. The alloy according to claim 10 wherein the alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 38% IACS.
14. The alloy according to claim 10 wherein the alloy is processed to have a yield strength of at least about 143 ksi , and an electrical conductivity of at least about 37% IACS.
15. The alloy according to claim 10 wherein the alloy is processed to have a yield strength of at least about 157 ksi, and an electrical conductivity of at least about 32% IACS.
16. The cooper base alloy according to claim 1 wherein the alloy is in the form of foil, wire, bar or tube.
17. A copper base alloy having an improved combination of yield strength, electrical conductivity, and formability, consisting essentially of:
between about 3.0 and about 5.0 weight percent Ni;
up to about 2.0 weight percent Co;
between about 0.7 and about 1.5 weight percent Si;
between about 0.03 and about 0.25 weight percent Mg;
up to about 0.6 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities, the ratio of (Ni+Co)/(Si−Cr/5) being between about 3 and about 7.
18. A copper base alloy having an improved combination of yield strength, electrical conductivity, and formability, consisting essentially of:
between about 3.0 and about 5.0 weight percent Ni;
up to about 2.0 weight percent Co;
between about 0.7 and about 1.5 weight percent Si;
between about 0.03 and about 0.25 weight percent Mg;
up to about 0.6 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities, the alloy processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 25% IACS.
19. The alloy according to claim 18 wherein the alloy is processed to have a yield strength of at least about 137 ksi, and an electrical conductivity of at least about 38% IACS.
20. The alloy according to claim 18 wherein the alloy is processed to have a yield strength of at least about 143 ksi, and an electrical conductivity of at least about 37% IACS.
21. The alloy according to claim 18 wherein the alloy is processed to have a yield strength of at least about 157 ksi, and an electrical conductivity of at least about 32% IACS.
22. A copper base alloy having an improved combination of yield strength, electrical conductivity, stress relaxation resistance, consisting essentially of:
between about 3.5 and about 3.9 weight percent Ni;
between about 0.8 and about 1.0 weight percent Co;
between about 1.0 and about 1.2 weight percent Si;
between about 0.05 and about 0.15 weight percent Mg;
up to about 0.1 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities, the alloy processed to have a yield strength of at least about 140 ksi, and an electrical conductivity of at least about 30% IACS.
23. The alloy according to claim 22 wherein the ratio of (Ni+Co)/(Si−Cr/5) is between about 3.5 and about 5.0.
24. The alloy according to claim 23 wherein the ration of Ni/Co is between about 3 and about 5.
25. The alloy according to claim 22 wherein the ration of Ni/Co is between about 3 and about 5.
26. A process for making a copper base alloy including nickel, silicon, cobalt and chromium, comprising:
melting and casting the alloy;
hot rolling from about 750° to about 1050° C.;
cold rolling to a convenient gauge for solutionizing;
solution annealing the alloy at between about 800° and about 1050° C. for from about 10 seconds to about one hour; and
subsequently quenching or rapidly cooling the alloy to ambient temperature to obtain an electrical conductivity of less than about 20% IACS (11.6 MS/m) and an equiaxed grain size of about 5-20 μm;
cold rolling the alloy for a 0 to about 75% reduction in thickness;
subjecting the alloy to an hardening anneal at about 300° to about 600° C. for about 10 minutes to about 10 hours;
subsequently cold rolling the alloy for an about 10 to about 75% reduction in thickness to finish gauge;
subjecting the alloy to a second age hardening anneal at 250 to about 500° C. for about 10 minutes to about 10 hours to achieve.
27. The process according to claim 26 further comprising an intermediate recrystallization anneal after the hot rolling.
28. The process according to claim 26 wherein the alloy consists essentially of between about 1.0 and about 6.0 weight percent Ni;
up to about 3.0 weight percent Co;
between about 0.5 and about 2.0 weight percent Si;
between about 0.01 and about 0.5 weight percent Mg;
up to about 1.0 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities.
29. The process according to claim 28 wherein the alloy consists essentially of:
between about 3.0 and about 5.0 weight percent Ni;
up to about 2.0 weight percent Co;
between about 0.7 and about 1.5 weight percent Si;
between about 0.03 and about 0.25 weight percent Mg;
up to about 0.6 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn, the balance being copper and unavoidable impurities.
30. The process according to claim 29 wherein the ratio of (Ni+Co)/(Si−Cr/5) being between about 3 and about 7.
31. The process according to claim 29 wherein the alloy comprises between about 3.5 and about 3.9 weight percent Ni;
between about 0.8 and about 1.0 weight percent Co;
between about 1.0 and about 1.2 weight percent Si;
between about 0.05 and about 0.15 weight percent Mg;
up to about 0.1 weight percent Cr;
up to about 1.0 weight percent Sn, and up to about 1.0 weight percent Mn,
the balance being copper and impurities.
US12/336,731 2007-12-21 2008-12-17 Copper-nickel-silicon alloys Abandoned US20090183803A1 (en)

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* Cited by examiner, † Cited by third party
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US20110240182A1 (en) * 2008-12-12 2011-10-06 Jx Nippon Mining & Metals Corporation Ni-Si-Co COPPER ALLOY AND MANUFACTURING METHOD THEREFOR
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US20140305679A1 (en) * 2011-12-28 2014-10-16 Yazaki Corporation Ultrafine conductor material, ultrafine conductor, method for preparing ultrafine conductor, and ultrafine electrical wire
US10329654B2 (en) * 2013-06-04 2019-06-25 Ngk Insulators, Ltd. Method for manufacturing copper alloy and copper alloy

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594221A (en) * 1985-04-26 1986-06-10 Olin Corporation Multipurpose copper alloys with moderate conductivity and high strength
US4728372A (en) * 1985-04-26 1988-03-01 Olin Corporation Multipurpose copper alloys and processing therefor with moderate conductivity and high strength
US20040079456A1 (en) * 2002-07-02 2004-04-29 Onlin Corporation Copper alloy containing cobalt, nickel and silicon
US20060196586A1 (en) * 2002-03-12 2006-09-07 The Furukawa Electric Co., Ltd. High-strength, high-conductivity copper alloy wire excellent in resistance to stress relaxation

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4664584B2 (en) * 2003-09-18 2011-04-06 株式会社神戸製鋼所 High strength copper alloy plate and method for producing high strength copper alloy plate
JP4754930B2 (en) * 2005-10-14 2011-08-24 Jx日鉱日石金属株式会社 Cu-Ni-Si based copper alloy for electronic materials

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594221A (en) * 1985-04-26 1986-06-10 Olin Corporation Multipurpose copper alloys with moderate conductivity and high strength
US4728372A (en) * 1985-04-26 1988-03-01 Olin Corporation Multipurpose copper alloys and processing therefor with moderate conductivity and high strength
US20060196586A1 (en) * 2002-03-12 2006-09-07 The Furukawa Electric Co., Ltd. High-strength, high-conductivity copper alloy wire excellent in resistance to stress relaxation
US20040079456A1 (en) * 2002-07-02 2004-04-29 Onlin Corporation Copper alloy containing cobalt, nickel and silicon
US7182823B2 (en) * 2002-07-05 2007-02-27 Olin Corporation Copper alloy containing cobalt, nickel and silicon
US20070131315A1 (en) * 2002-07-05 2007-06-14 Olin Corporation And Wieland-Werke Ag Copper alloy containing cobalt, nickle and silicon

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110240182A1 (en) * 2008-12-12 2011-10-06 Jx Nippon Mining & Metals Corporation Ni-Si-Co COPPER ALLOY AND MANUFACTURING METHOD THEREFOR
US9394589B2 (en) * 2008-12-12 2016-07-19 Jx Nippon Mining & Metals Corporation Ni-Si-Co copper alloy and manufacturing method therefor
EP2508633A1 (en) * 2009-12-02 2012-10-10 Furukawa Electric Co., Ltd. Copper alloy sheet and process for producing same
EP2508633A4 (en) * 2009-12-02 2014-07-23 Furukawa Electric Co Ltd Copper alloy sheet and process for producing same
US20140305679A1 (en) * 2011-12-28 2014-10-16 Yazaki Corporation Ultrafine conductor material, ultrafine conductor, method for preparing ultrafine conductor, and ultrafine electrical wire
US9214252B2 (en) * 2011-12-28 2015-12-15 Yazaki Corporation Ultrafine conductor material, ultrafine conductor, method for preparing ultrafine conductor, and ultrafine electrical wire
US10329654B2 (en) * 2013-06-04 2019-06-25 Ngk Insulators, Ltd. Method for manufacturing copper alloy and copper alloy

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