CA1237361A - Thermomechanical processing of beryllium-copper alloys - Google Patents
Thermomechanical processing of beryllium-copper alloysInfo
- Publication number
- CA1237361A CA1237361A CA000465690A CA465690A CA1237361A CA 1237361 A CA1237361 A CA 1237361A CA 000465690 A CA000465690 A CA 000465690A CA 465690 A CA465690 A CA 465690A CA 1237361 A CA1237361 A CA 1237361A
- Authority
- CA
- Canada
- Prior art keywords
- alloy
- nickel
- accordance
- beryllium
- tensile strength
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229910000881 Cu alloy Inorganic materials 0.000 title claims abstract description 15
- DMFGNRRURHSENX-UHFFFAOYSA-N beryllium copper Chemical compound [Be].[Cu] DMFGNRRURHSENX-UHFFFAOYSA-N 0.000 title claims abstract description 14
- 230000000930 thermomechanical effect Effects 0.000 title claims abstract description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 81
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 42
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 41
- 239000000956 alloy Substances 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 22
- 229910052790 beryllium Inorganic materials 0.000 claims abstract description 15
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 14
- 239000010941 cobalt Substances 0.000 claims abstract description 14
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 14
- 230000032683 aging Effects 0.000 claims abstract description 13
- 238000002844 melting Methods 0.000 claims abstract description 10
- 230000008018 melting Effects 0.000 claims abstract description 10
- 238000005482 strain hardening Methods 0.000 claims abstract description 4
- 239000012535 impurity Substances 0.000 claims description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- 239000010949 copper Substances 0.000 claims description 7
- 229910052709 silver Inorganic materials 0.000 claims description 7
- 239000004332 silver Substances 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 229910052726 zirconium Inorganic materials 0.000 claims description 5
- 238000001556 precipitation Methods 0.000 claims description 4
- 229910000892 beryllide Inorganic materials 0.000 claims description 3
- 238000000137 annealing Methods 0.000 abstract description 21
- 239000000243 solution Substances 0.000 description 22
- 239000000463 material Substances 0.000 description 16
- 239000002244 precipitate Substances 0.000 description 10
- 239000011133 lead Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000005275 alloying Methods 0.000 description 4
- 238000004881 precipitation hardening Methods 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 241001124569 Lycaenidae Species 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 235000014987 copper Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000005473 Guinier-Preston zone Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000002547 anomalous effect Effects 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000003483 aging Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Conductive Materials (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Physical Vapour Deposition (AREA)
Abstract
Abstract of the Disclosure The invention contemplates a thermomechanical process applicable to beryllium copper alloys containing, by weight, about 0.1% to about 1.2%
beryllium, at least about 0.1% to about 3.5% nickel, up to about 3% cobalt, with the total content of nickel and cobalt being about 0.5% to about 3.5%, which process comprises solution annealing said alloy at a temperature of at least about 90% of the incipient melting point in °F. therefor, cold working the solution treated alloy to reduce the section thickness at least about 60% or much more and then aging the alloy to produce therein an improved combination of properties including strength, ductility, formability and conductivity.
beryllium, at least about 0.1% to about 3.5% nickel, up to about 3% cobalt, with the total content of nickel and cobalt being about 0.5% to about 3.5%, which process comprises solution annealing said alloy at a temperature of at least about 90% of the incipient melting point in °F. therefor, cold working the solution treated alloy to reduce the section thickness at least about 60% or much more and then aging the alloy to produce therein an improved combination of properties including strength, ductility, formability and conductivity.
Description
~73~
THERMOMECHANICAL PROCESSING OF BERYLLIU~-COPPER ALLOYS
The present invention is directed to a thermomechanical process for improv-ing the mechanical properties of beryllium-copper alloys and to the product re-sulting therefrom.
Backqround of the Invention and the Prior Art -- . .
Beryllium-copper alloys having a variety of compositions and presenting a range of properties, both mechanical and electrical, are known. Such alloys may contain beryllium in ~he range of about 0.1% to about 3% to confer age harden-ability through a precipitation hardening heat treatment and may contain small amounts of other alloying ingredients such as cobalt~ nickel, silver, etc. for special purposes. The alloys in strip form are useful for the production of connectors, switch parts, relays and many other parts amenable to production in progressive dies. In rod, bar, tube and plate form the alloys find use in ma-chined connectors, welding electrodes, injection molding tooling and similar ap-plications. As uses of the alloys have progressed, a demand has arisen ~or stronger alloys which would still retain significant ductility~ electrical con-ductivity~ formability and other desirable properties. For e~ample, the strength of the alloys can be increased by application of cold work in amounts up to possibly 37%, e.g., 21%, after precipitation hardening, but such a prac-tice reduces the ductility and formability of the material and, in addition, electrical conductivity is also degraded. On the other hand, increases in conductivity may be achieved by substantial overaging, but at the expense of strengthO
Heat treatment of the alloys usually involves a solution annealing treat-ment to insure solid solution of the alloying elements added for strengthening, and a precipitation-hardening ~aging) heat treatment. Solution annealing of the .
3~
--~3~3~
alloys is conducted commercially at a temperature in the range of about 1325 F to about 1650 F forshort periods, e.g., about 5 minutes. A quench, e.g., a water quench, is employed after solution treating to retain alloying elements in solution.
Aging is usually conducted in the temperature range of about 450 F to about 925 F for periods of up to about 4 hours.
The invention is directed to a thermomechanical process for providing, in certain beryllium-copper alloys, improved strength, ductility and formability as compared to the properties attainable by prior procedures, without degradation of conductivity.
Summary of the Invention Beryllium copper alloys containing about 0.2% to about 0.7% beryllium, about 1.0 to about 3.5% of nickel and cobalt, where nickel constitutes greater than a trace amount, e.g., at least 1.0% Ni, in the aggregate, small amounts of zirconium, lead, magnesium, silver and incidental impurities and the balance essentially copper are processed by solution anneal-ing at a temperature at least 90% of the incipient melting temperature of the alloy sufficient to form a previously unre-ported fine dispersion of nickel-rich precipitate phase, cold working the solution annealed alloy to effect a reduction in excess of about 60%, and thereafter aging the cold-worked alloy to impart thereto an improve~ combination of mechanical propert-ies includingstrength and ductility, Formability and electrical conductivity.
THERMOMECHANICAL PROCESSING OF BERYLLIU~-COPPER ALLOYS
The present invention is directed to a thermomechanical process for improv-ing the mechanical properties of beryllium-copper alloys and to the product re-sulting therefrom.
Backqround of the Invention and the Prior Art -- . .
Beryllium-copper alloys having a variety of compositions and presenting a range of properties, both mechanical and electrical, are known. Such alloys may contain beryllium in ~he range of about 0.1% to about 3% to confer age harden-ability through a precipitation hardening heat treatment and may contain small amounts of other alloying ingredients such as cobalt~ nickel, silver, etc. for special purposes. The alloys in strip form are useful for the production of connectors, switch parts, relays and many other parts amenable to production in progressive dies. In rod, bar, tube and plate form the alloys find use in ma-chined connectors, welding electrodes, injection molding tooling and similar ap-plications. As uses of the alloys have progressed, a demand has arisen ~or stronger alloys which would still retain significant ductility~ electrical con-ductivity~ formability and other desirable properties. For e~ample, the strength of the alloys can be increased by application of cold work in amounts up to possibly 37%, e.g., 21%, after precipitation hardening, but such a prac-tice reduces the ductility and formability of the material and, in addition, electrical conductivity is also degraded. On the other hand, increases in conductivity may be achieved by substantial overaging, but at the expense of strengthO
Heat treatment of the alloys usually involves a solution annealing treat-ment to insure solid solution of the alloying elements added for strengthening, and a precipitation-hardening ~aging) heat treatment. Solution annealing of the .
3~
--~3~3~
alloys is conducted commercially at a temperature in the range of about 1325 F to about 1650 F forshort periods, e.g., about 5 minutes. A quench, e.g., a water quench, is employed after solution treating to retain alloying elements in solution.
Aging is usually conducted in the temperature range of about 450 F to about 925 F for periods of up to about 4 hours.
The invention is directed to a thermomechanical process for providing, in certain beryllium-copper alloys, improved strength, ductility and formability as compared to the properties attainable by prior procedures, without degradation of conductivity.
Summary of the Invention Beryllium copper alloys containing about 0.2% to about 0.7% beryllium, about 1.0 to about 3.5% of nickel and cobalt, where nickel constitutes greater than a trace amount, e.g., at least 1.0% Ni, in the aggregate, small amounts of zirconium, lead, magnesium, silver and incidental impurities and the balance essentially copper are processed by solution anneal-ing at a temperature at least 90% of the incipient melting temperature of the alloy sufficient to form a previously unre-ported fine dispersion of nickel-rich precipitate phase, cold working the solution annealed alloy to effect a reduction in excess of about 60%, and thereafter aging the cold-worked alloy to impart thereto an improve~ combination of mechanical propert-ies includingstrength and ductility, Formability and electrical conductivity.
- 2 -~. ~
1~3~36~l.
53~-815 Thus, an aspect of the present invention provides a thermomechanical process for obtaining improved combinations o-E properties in beryllium copper alloys consisting essentially of, all by weight, about 1.0% to about 3.5% nickel and cobalt in the aggregate, wi*h at least about 1.0% nickel; about 0.2%
to about 0.7% beryllium; up to about 1.0% zirconium; up to about 0.005% lead; up to 0.1% magnesium; up to about 1.5% silver and up to about 0.5% incidental impurities including lead; and the balance essentially copper, which process comprises the steps of solution treating the alloy at a temperature within about 90%
of the incipient melting temperature therefor expressed in degrees Farenheit to effect precipitation of a fine dispersion of a nickel~rich phase, cold working the solution treated alloy to reduce the section thickness thereof at least about 60% and thereafter aging the cold worked alloy at a temperature of about 600 to about 900F. to produce in said alloy in the condition resulting from said aging an improved comhination of properties including strength, ductility and electrical conductivity, which on a graph of ultimate tensile strength versus elongation line along or above a line connectingthe points defined by 150 ksi ultimate tensile strength at 3~5% elongation and 120 ksi ultimate tensile strengkh at 15% elongation.
Another aspect of the present invention provides rod, bar, tube, plate, strip and wire made of an age hardenable alloy consisting essentially of at least about 1.0 wt% to about
1~3~36~l.
53~-815 Thus, an aspect of the present invention provides a thermomechanical process for obtaining improved combinations o-E properties in beryllium copper alloys consisting essentially of, all by weight, about 1.0% to about 3.5% nickel and cobalt in the aggregate, wi*h at least about 1.0% nickel; about 0.2%
to about 0.7% beryllium; up to about 1.0% zirconium; up to about 0.005% lead; up to 0.1% magnesium; up to about 1.5% silver and up to about 0.5% incidental impurities including lead; and the balance essentially copper, which process comprises the steps of solution treating the alloy at a temperature within about 90%
of the incipient melting temperature therefor expressed in degrees Farenheit to effect precipitation of a fine dispersion of a nickel~rich phase, cold working the solution treated alloy to reduce the section thickness thereof at least about 60% and thereafter aging the cold worked alloy at a temperature of about 600 to about 900F. to produce in said alloy in the condition resulting from said aging an improved comhination of properties including strength, ductility and electrical conductivity, which on a graph of ultimate tensile strength versus elongation line along or above a line connectingthe points defined by 150 ksi ultimate tensile strength at 3~5% elongation and 120 ksi ultimate tensile strengkh at 15% elongation.
Another aspect of the present invention provides rod, bar, tube, plate, strip and wire made of an age hardenable alloy consisting essentially of at least about 1.0 wt% to about
3.5 wt~ nickel and cobalt in the aggregate, with at least about 1~3~36 3L.
0.2 wt~ to about 0.7 wt% beryllium; up to about 1.0 wt%
zirconium; up to about 0.005 wt% lead; up to 0.1 wt% ~agnesium;
up to about 1.5 wt% silver; and up to about 0.5 wt% incidental impurities including lead; and the balance essentiall~ copper;
having (a) a textured grain orientation, (b) a yield strength higher in the transverse direc-tion than in the longitudinal direction, (c) a microstructure including an optically resolvable nickel-rich phase distinct from the primary beryllide and the principal hardening phases, and (d) an improved combination of properties including strength, ductility and electrical conductivity; which on a graph o ultimate tensile strength versus elongation will lie along or above a line connecting the points defined by 149 ksi ultimate tensile strength at 2 elongation and 100 ksi ultimate tensile strength at 15%
elongation.
Description of the Drawing The drawing shown in Figure 1 depicts the vptical microstructure, taken at 1000 diameters in the longitudinal orientation, of a strip product provided in accordance with the invention. Transmission electron micrographs are also shown in Figure 2 (a) and 2 (b) at 18,OOOX and 141,000X respectively, showing the nickel-rich precipitates, identified as A~ and the principal hardening phases, identified as B, consisting of Guinier-Preston zones and ~" precipitates~
- 3a -1~:3~36~.
Detailed Description of the Invention Alloy products provided in accordance with the invention contain, in addition to copper, beryllium and nickel as essential ingredients with beryllium being in the range, by weight, of about 0.2% to about 0.7%. Cobalt and nickel are present in combination in the range of about 1.0~ to about 3.5%, preferably about 0.1% to about 2.5%, where nickel constitutes greater than a trace amount, e.g., over about 1.0% Ni. Magnesium and silver are pLesent in the range of up to 0.1% and about 1.5%, respectivelyO Other incidental elements and impurities may be present in a total amount of about 0.5% maximum including of up to about 0.005~ lead. Such elements and impurities include silicon, iron, aluminum, tin, zinc, chromium, lead, phosphorus, sulfur, etc. They should not generally be present in amounts exceeding 0.1% each, more preferahly in amounts less tha 0.01%
each, or even lower, as ~hese elements are detrimental to electrical conductivity or mechanical properties.
Conveniently, solution annealing is performed when the material is at a ready-to-finish gaye. Solution annealing time is only that re~uired to thoroughly heat through the section being treated. A rapid quench from the annealing temperature, e.g./ an atmosphere or a water quench, is employed.
Alloys treated in accordance with the invention usually will have an incipient melting point (measured in degrees F) of at least about 1830 F. In carrying out the invention, the ~ 3b -~.
~3~3~.
solution annealing is conducted at a temperature of at least about 90% of the incipient melting point for the alloy (measured in degrees F) to effect the precipitation of a fine dispersion of a nickel-rich phase. Advantageously, solution annealing is conducted at 92%, or even at 95% of the incipient melting point of the alloy measured in degrees F. Incipient melting, however, should be avoided. The solution-annealed alloy is then cold-worked to effect a high reduction in excess of about 60%, e.g., about 75%, 3c -~L~3~36~. ( or 80%, or 90% or more, without an intermediate anneal. The highly cold-worked material, usually in strip form, is then aged usually in the tempera-ture range of about 600 F to about 900 F for up to 4 hours, e.g., about 2 to about 8 hours.Optimum aging times and temperatures within these ranges are dictated by composition and the property levels desired in the product.
The solution annealed material is characterized by a fine dispersion of nickel-rich precipitates which raise as-annealed hardness and contribute to inhibition of grain growth. The cold worked solution annealed material is characterized by a texture or preferred grain orientation which results in obtaining a yield strength which is higher in the transverse clirection than in the longitudinal direction. The textured grain orientation in the heavily cold worked alloy product of the invention is evident in the drawing (Figure 1), as is the precipitation of a nickel-rich phase appearing in random distribution as dark spots in Figure 1 and as discrete particles ~identified as A) in the size range 0.13-0.25 micron in Figure 2 (a) and Figure 2 (b). The principal hardening phases are much more difficult to resolve in the optical microscope but can be detected using techniques such as transmission electron microscopy asshown in Figure 2 (a) and Figure 2 (b). They (identified as B in Figure 2 (a) and Figure 2 (b)) consist of Guinier-Preston zones and ~q", as finely dispersed particles 50 to 100 A in diameter. The copper-base material from which the drawing was taken was 0.008 inch thick strip of an alloy which contained 0.42%
B~, 1.70% Ni which had been solution annealed at 0.080 inch thickness at a temperature of 1800 F, had been cold worked 90% and aged 4 hours at 750 F.
In order to illustrate the advantages of the invention, the following exam-ples are given:
73~
Example 1 A notable feature of the invention is that the annealed hardness increases in an unexpected manner above the solution annealing temperature at which the nickel-rich precipitate particles form. To illustrate the anomalous hardening of the alloys containing nickel in greater than trace amounts, e.g., over 0.1%
Ni, strip samples of varying compositions were quenched after holding 1 hour at the solution annealing temperatures of 1650 F and 1800 Fo Hardness and microstructural observations were made in the as-quenched condition. The results are set forth in Table 1 and Table 2.
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~ ~23~3G~. ( Example 2 Several heats were prepared having the compositions (wt%) set forth in Table 3:
1,~ 3.~S
Heat C Heat D Heat E Heat F Heat G Heat H
Wt% Wt~ Wt% Wt% Wt% Wt%
Be 0.63 0.58 0.50 0.42 0.40 0.42 Ni 0.01 0.01 1.00 1.70 1.91 1.64 Co 2.50 2.62 1.00 <0.01 0.005 0.05 Fe 0.04 0.05 0.03 <0.01 <0.01 0.06 Si 0.04 0.04 0.02 0.02 <0.01 0.07 Al 0.02 0.02 <0.01 <0.01 <0.01 0.03 Sn 0.006 0.012 <0.003 <0O005 <0.005 0.01 Zn <0.01 <0.01 <0.01 <0.01 <0.01 <0.01 Cr <0.005 <0.005 <0.005 <0.005 <0-005 <0-005 Pb <0.003 <0.003 <0.003 <C.003 <0.003 <0.003 p <0.005 <0.005 <0.005 0.001 <0.005 <0.005 Cu Bal. Bal. Bal. Bal. Bal. Bal.
C ~3~3~
The commercial weight ingot material from Heat F was hot rolled to 0.8 inch plate. Four pieces of 0.8 inch plate from Heat F were solution annealed respectively at 1750 F, 1800 F, 1825 F and 1850 F for 45 minutes and water quenched. Each plate was cold rolled 90% to 0.082 lnch thick, and cut into three pieces which were then aged 4 hours at respective temperatures of 750 F, 800 F and 850 F in argon.
Standard tensile specimens were prepared from the aged strip. All materials were tested in the longitudinal direction and certain materials were also tested in the transverse direction. Electrical conductivity was measured at room temperature.
Results from Heat F are given in Table 4:
1 n .~ . o~ .o ~ O .0 . ~ .o NU`) COU~ n~ Oo O . ~
C~ o . _ O ~ o ~ o o . o ~ o ui n . O _ _ _ o o _ A D Z ~o Z n z ~n z ~n z n z u~ z n z n ~r> n n ~ u~ n u~ n z ~ z ~ ~) r~ o_q ~ O .0 ~ 0~ 00~ O O C~J o C~1 'J o ~~
N Vl ~ -- U N Z C~l Z ~J Z C~l Z ~ Z C~l Z ~ Z N Z ~ ~ N ~) Z ~ Z 1'-) Z ~ Z
o ~ u cn o~ ~ ~ O ~ ~ u~ ~r r~ ~ n D G~ D N lD ~t ~ ~ 1~ ~ 0 ~ O CO
0: ~c ~ n __~__ C~i__a~ _O~ __ c~r~ I~c~ 1~1~ ~
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L~ = O__~ OO~O~ ~?n~o~o -~ ~r7 ~7 ;~ L C~ _C t~ n U~> _ ~ ~ o r~ n n ~ co--~ ~ ~D o ~D C:) ~ o ~ o t _~ ~a ~ - ~ ~ ~ ~ ~ ~ c~
LJ C _ V. C~l C C C~. Cl C C V. ~1 C C Cl. C7'. C C C'. C. Cl~ C~'. Gl U'. CJ. Cll C~ Vl C C
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O~ ~ o o o o ~ oo cOo W o o n O O O u) O Il') C E ¦ -- O~ _ _ _ _ _ W ~
-10~
C ~ 3~36~. ( Example 3 Material from Heat G was processed as a commercial weight coil by hot rolling, annealing, surface conditioning and cold rolling to an intermediate thickness of 0.060 inch. The cold rolled 0.060 inch strip at a width of 7.5 inches was strand solution annealed at 1800 F. The annealed strip was then finish rolled to about 0.0083 inches, a reduction of approximately 90%. Tensile specimens were cut from the strip in both longitudinal and transverse directions and aged in argon at 700 F, 750 F, 800 F and 850 F. One set was aged for four hours and one set was aged for 8 hours. Tensile properties, formability and conductivity were obtained. Formability was determined on the thin strip specimens by bending 90 around punches having successively smaller radii until cracking occurred on the tensiie surface of the bend. The minimum bend radius, kaken as the smallest radius which can be used without cracking, was expressed in multiples of strip thickness.
Results from Heat G are set forth in the following Table 5, in which mechanical properties reported are based on the average of duplicate tests:
{ ~3~3~ ~
'O ~11'7 C~l U~ ~1 ~) el N ~r Ir> ~ N C 10 ~ N U~
N _ N _ N l N 1~ _ C~ O ~ _ N
' ~ CC --l _ ~ N
,~0 _ _ __ _ ._ ~ ~) 1'-7 CO 1~ ~ ~D N O .~ ~D ~ 1 iO
C) o ~R ~ 'J ~ ~ N _1 Il~ U~ ~J O U'~ U') N N
..JO __ .~
>~ C) ~ r ~ ~D U~ ~ ~O ~`q _ _ C ~ _ _ ~r O
Q. O T*~ ~N N O O N N O O N N ~I N N N
C~: .~
~ OS __ ~~' ' Ll a~ N ~0 O ~ Cl ~ U'l CO a:~ ~ ~) _I ~57 _I 1~
u cl~ _ u~~ o ~ _. _ ,~ _ c~ 5'1 a~ co ~n v~v _ _ ~a~ ~-D ~_ COI~ 00 0~ ~0 O~D r~o .1 ~ Vl Vl _ _ .D O ~ r-~ N ~ _ _ _ ~ _ _ N ~
I.J CJ , o _ _ cv,~ c .
L N O O O V~ O~ CO ~_ 11-1 D ~ O ~ I'_ U7 0 <!:1 V' N U7 N ~ V- ~D O. N _ _I ~ _ ~ N ~ N .
l_ .
. -,0 .V .V .V .V V' V' .V .V.
~ cc. 0 C 0 C~ 0 C~ 0 C~ 0 cV~ 0 C~ 0 C~ 0 ._ ~ L _ 1- ~_ _ l_ ~ _ ~- _ ~- _ l-O ~ _~ L~ ~ L~ _ ~
E o o O o o o o o V L L L L L L L L
0 ~ :~ ~ ~ ~ c~ c a~
7363l.
Example 4 Materials from Heats C, D, E and H having a variety of compositions were processed similar to Heat G in Example 3. Strip materials at a ready-to-finish gage ranging from 0.020-0.060 in. were solution annealed at 1800 F. The annealed strip was finish rolled to effect a reduction of approximately 90%.
Specimens were sectioned in the longitudinal orientation and aged for four hours at 750 F in argon. Tensile properties and electrical conductivity were obtained at room temperature. The results are set forth in Table 6.
.
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aJ o ~ o Lr~ o ~ O ~ o ~ L oc o~ oo ~3'7~
The data of Table 1 show that beryllium-copper alloys containing nickel in excess of trace a~ounts experience an increase in as-annealed hardness with increasing annealing temperature, whereas beryllium copper alloys containina cobalt with only trace amounts of nickel continue to soften with increasing annealing temperature. The reason for this anomalous hardness increase is apparent from Table 2. At annealing temperatures near 1800 F, the nickel-containing beryllium coppers of Table 2 (i.e., Heats A, B and E) form a nickel-rich precipitate which is distinct from both the primary beryllide phase and the principal hardening phase as illustrated in Figures 1 and 2. The cobalt-containing beryllium coppers of Table 2 (i.e., Heats C and D) do not formsuch precipitates at the higher annealing temperature. These nickel-rich precipitates are believed to contribute to the enhanced mechanical and physical -properties of the alloys processed per this invention through: (a) strengtheningof the matrix by dispersion hardening, (b) ductility improvement through inhibition of grain growth at the high annealing temperature and (c) improvementin conductivity through depletion of alloying elements in solid solution.
An additional reason for the improved properties provided in accordance with the invention has to do with the high volume fraction of coherent principalhardening precipitates which forms on aging of material previously subjected to the high solution annealing temperature and substantial cold work. The high solution annealing treatment dissolves more beryllium and nickel plus cobalt in the copper matrix, thereby providing more material available to precipitate on aging. The heavy cold work provides a deformation texture contributing to the high strength.
3~i1 ( Inspection of the data in Tables 4, 5 and 6 indicates that the best combi-nations of strength and ductility resulted from the combination of (a) presence of nickel over a trace amount, (b) annealing temperatures of at least 1800 F and ~c) aging at 750 F. Property combinations including 140,000 psi yield strength, 10% elongation and a conductivity near 50% IACS were obtained. Conductivity and formability were improved by the 8-hour aging time. It is to be appreciated that the alloys tested in Tables 4 and 5 contained less than 0.01% each of iron, cobalt and aluminum and that this low impurity level contributes significantly to electrical conductivity. Nevertheless, strip material of comparable composi-tion conventionally processed by cold rolling even as much as 37% to full hard temper after age hardening to a yield strength of approximately 140,000 psi would be found to have an elongation not exceeding 2%, with poorer formability and lower conductivity. Conversely, material of similar composition subjected to overaging to achieve 60% IACS minimum conductivity would exhibit less than 75,000 psi yield strength.
The data of Table 6 clearly show that cobalt-containing beryllium coppers with only trace amounts of nickel do not respond as favorably to the processing of this invention as do their nickel-containing counterparts.
It is to be further appreciated that the properties reported in Tables 4, 5 and 6 are dependent upon the beryllium and nickel contents of the example heats.
Different chemistries within the ranges defined will yield different property levels, but it is believed that, when processed according to the teachings of the invention, these compositions will yield superior properties compared to the same alloys conventionally processed. Once formed the nickel-rich precipitates described above appear to remain stable and to resist resolution on subsequent reannealing suggesting that additional advantages may accrue from annealing at high temperatures at various process points.
0.2 wt~ to about 0.7 wt% beryllium; up to about 1.0 wt%
zirconium; up to about 0.005 wt% lead; up to 0.1 wt% ~agnesium;
up to about 1.5 wt% silver; and up to about 0.5 wt% incidental impurities including lead; and the balance essentiall~ copper;
having (a) a textured grain orientation, (b) a yield strength higher in the transverse direc-tion than in the longitudinal direction, (c) a microstructure including an optically resolvable nickel-rich phase distinct from the primary beryllide and the principal hardening phases, and (d) an improved combination of properties including strength, ductility and electrical conductivity; which on a graph o ultimate tensile strength versus elongation will lie along or above a line connecting the points defined by 149 ksi ultimate tensile strength at 2 elongation and 100 ksi ultimate tensile strength at 15%
elongation.
Description of the Drawing The drawing shown in Figure 1 depicts the vptical microstructure, taken at 1000 diameters in the longitudinal orientation, of a strip product provided in accordance with the invention. Transmission electron micrographs are also shown in Figure 2 (a) and 2 (b) at 18,OOOX and 141,000X respectively, showing the nickel-rich precipitates, identified as A~ and the principal hardening phases, identified as B, consisting of Guinier-Preston zones and ~" precipitates~
- 3a -1~:3~36~.
Detailed Description of the Invention Alloy products provided in accordance with the invention contain, in addition to copper, beryllium and nickel as essential ingredients with beryllium being in the range, by weight, of about 0.2% to about 0.7%. Cobalt and nickel are present in combination in the range of about 1.0~ to about 3.5%, preferably about 0.1% to about 2.5%, where nickel constitutes greater than a trace amount, e.g., over about 1.0% Ni. Magnesium and silver are pLesent in the range of up to 0.1% and about 1.5%, respectivelyO Other incidental elements and impurities may be present in a total amount of about 0.5% maximum including of up to about 0.005~ lead. Such elements and impurities include silicon, iron, aluminum, tin, zinc, chromium, lead, phosphorus, sulfur, etc. They should not generally be present in amounts exceeding 0.1% each, more preferahly in amounts less tha 0.01%
each, or even lower, as ~hese elements are detrimental to electrical conductivity or mechanical properties.
Conveniently, solution annealing is performed when the material is at a ready-to-finish gaye. Solution annealing time is only that re~uired to thoroughly heat through the section being treated. A rapid quench from the annealing temperature, e.g./ an atmosphere or a water quench, is employed.
Alloys treated in accordance with the invention usually will have an incipient melting point (measured in degrees F) of at least about 1830 F. In carrying out the invention, the ~ 3b -~.
~3~3~.
solution annealing is conducted at a temperature of at least about 90% of the incipient melting point for the alloy (measured in degrees F) to effect the precipitation of a fine dispersion of a nickel-rich phase. Advantageously, solution annealing is conducted at 92%, or even at 95% of the incipient melting point of the alloy measured in degrees F. Incipient melting, however, should be avoided. The solution-annealed alloy is then cold-worked to effect a high reduction in excess of about 60%, e.g., about 75%, 3c -~L~3~36~. ( or 80%, or 90% or more, without an intermediate anneal. The highly cold-worked material, usually in strip form, is then aged usually in the tempera-ture range of about 600 F to about 900 F for up to 4 hours, e.g., about 2 to about 8 hours.Optimum aging times and temperatures within these ranges are dictated by composition and the property levels desired in the product.
The solution annealed material is characterized by a fine dispersion of nickel-rich precipitates which raise as-annealed hardness and contribute to inhibition of grain growth. The cold worked solution annealed material is characterized by a texture or preferred grain orientation which results in obtaining a yield strength which is higher in the transverse clirection than in the longitudinal direction. The textured grain orientation in the heavily cold worked alloy product of the invention is evident in the drawing (Figure 1), as is the precipitation of a nickel-rich phase appearing in random distribution as dark spots in Figure 1 and as discrete particles ~identified as A) in the size range 0.13-0.25 micron in Figure 2 (a) and Figure 2 (b). The principal hardening phases are much more difficult to resolve in the optical microscope but can be detected using techniques such as transmission electron microscopy asshown in Figure 2 (a) and Figure 2 (b). They (identified as B in Figure 2 (a) and Figure 2 (b)) consist of Guinier-Preston zones and ~q", as finely dispersed particles 50 to 100 A in diameter. The copper-base material from which the drawing was taken was 0.008 inch thick strip of an alloy which contained 0.42%
B~, 1.70% Ni which had been solution annealed at 0.080 inch thickness at a temperature of 1800 F, had been cold worked 90% and aged 4 hours at 750 F.
In order to illustrate the advantages of the invention, the following exam-ples are given:
73~
Example 1 A notable feature of the invention is that the annealed hardness increases in an unexpected manner above the solution annealing temperature at which the nickel-rich precipitate particles form. To illustrate the anomalous hardening of the alloys containing nickel in greater than trace amounts, e.g., over 0.1%
Ni, strip samples of varying compositions were quenched after holding 1 hour at the solution annealing temperatures of 1650 F and 1800 Fo Hardness and microstructural observations were made in the as-quenched condition. The results are set forth in Table 1 and Table 2.
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~ ~23~3G~. ( Example 2 Several heats were prepared having the compositions (wt%) set forth in Table 3:
1,~ 3.~S
Heat C Heat D Heat E Heat F Heat G Heat H
Wt% Wt~ Wt% Wt% Wt% Wt%
Be 0.63 0.58 0.50 0.42 0.40 0.42 Ni 0.01 0.01 1.00 1.70 1.91 1.64 Co 2.50 2.62 1.00 <0.01 0.005 0.05 Fe 0.04 0.05 0.03 <0.01 <0.01 0.06 Si 0.04 0.04 0.02 0.02 <0.01 0.07 Al 0.02 0.02 <0.01 <0.01 <0.01 0.03 Sn 0.006 0.012 <0.003 <0O005 <0.005 0.01 Zn <0.01 <0.01 <0.01 <0.01 <0.01 <0.01 Cr <0.005 <0.005 <0.005 <0.005 <0-005 <0-005 Pb <0.003 <0.003 <0.003 <C.003 <0.003 <0.003 p <0.005 <0.005 <0.005 0.001 <0.005 <0.005 Cu Bal. Bal. Bal. Bal. Bal. Bal.
C ~3~3~
The commercial weight ingot material from Heat F was hot rolled to 0.8 inch plate. Four pieces of 0.8 inch plate from Heat F were solution annealed respectively at 1750 F, 1800 F, 1825 F and 1850 F for 45 minutes and water quenched. Each plate was cold rolled 90% to 0.082 lnch thick, and cut into three pieces which were then aged 4 hours at respective temperatures of 750 F, 800 F and 850 F in argon.
Standard tensile specimens were prepared from the aged strip. All materials were tested in the longitudinal direction and certain materials were also tested in the transverse direction. Electrical conductivity was measured at room temperature.
Results from Heat F are given in Table 4:
1 n .~ . o~ .o ~ O .0 . ~ .o NU`) COU~ n~ Oo O . ~
C~ o . _ O ~ o ~ o o . o ~ o ui n . O _ _ _ o o _ A D Z ~o Z n z ~n z ~n z n z u~ z n z n ~r> n n ~ u~ n u~ n z ~ z ~ ~) r~ o_q ~ O .0 ~ 0~ 00~ O O C~J o C~1 'J o ~~
N Vl ~ -- U N Z C~l Z ~J Z C~l Z ~ Z C~l Z ~ Z N Z ~ ~ N ~) Z ~ Z 1'-) Z ~ Z
o ~ u cn o~ ~ ~ O ~ ~ u~ ~r r~ ~ n D G~ D N lD ~t ~ ~ 1~ ~ 0 ~ O CO
0: ~c ~ n __~__ C~i__a~ _O~ __ c~r~ I~c~ 1~1~ ~
~ ~ __I~D o n~ ~D o n~o Lr~ ~ I~ oo c~o O co ~r~
L~ = O__~ OO~O~ ~?n~o~o -~ ~r7 ~7 ;~ L C~ _C t~ n U~> _ ~ ~ o r~ n n ~ co--~ ~ ~D o ~D C:) ~ o ~ o t _~ ~a ~ - ~ ~ ~ ~ ~ ~ c~
LJ C _ V. C~l C C C~. Cl C C V. ~1 C C Cl. C7'. C C C'. C. Cl~ C~'. Gl U'. CJ. Cll C~ Vl C C
U ~ J C o O ~ ~ O O L L C C 0 _ _ ~ C C C C C C C C C C
.~ .
O~ ~ o o o o ~ oo cOo W o o n O O O u) O Il') C E ¦ -- O~ _ _ _ _ _ W ~
-10~
C ~ 3~36~. ( Example 3 Material from Heat G was processed as a commercial weight coil by hot rolling, annealing, surface conditioning and cold rolling to an intermediate thickness of 0.060 inch. The cold rolled 0.060 inch strip at a width of 7.5 inches was strand solution annealed at 1800 F. The annealed strip was then finish rolled to about 0.0083 inches, a reduction of approximately 90%. Tensile specimens were cut from the strip in both longitudinal and transverse directions and aged in argon at 700 F, 750 F, 800 F and 850 F. One set was aged for four hours and one set was aged for 8 hours. Tensile properties, formability and conductivity were obtained. Formability was determined on the thin strip specimens by bending 90 around punches having successively smaller radii until cracking occurred on the tensiie surface of the bend. The minimum bend radius, kaken as the smallest radius which can be used without cracking, was expressed in multiples of strip thickness.
Results from Heat G are set forth in the following Table 5, in which mechanical properties reported are based on the average of duplicate tests:
{ ~3~3~ ~
'O ~11'7 C~l U~ ~1 ~) el N ~r Ir> ~ N C 10 ~ N U~
N _ N _ N l N 1~ _ C~ O ~ _ N
' ~ CC --l _ ~ N
,~0 _ _ __ _ ._ ~ ~) 1'-7 CO 1~ ~ ~D N O .~ ~D ~ 1 iO
C) o ~R ~ 'J ~ ~ N _1 Il~ U~ ~J O U'~ U') N N
..JO __ .~
>~ C) ~ r ~ ~D U~ ~ ~O ~`q _ _ C ~ _ _ ~r O
Q. O T*~ ~N N O O N N O O N N ~I N N N
C~: .~
~ OS __ ~~' ' Ll a~ N ~0 O ~ Cl ~ U'l CO a:~ ~ ~) _I ~57 _I 1~
u cl~ _ u~~ o ~ _. _ ,~ _ c~ 5'1 a~ co ~n v~v _ _ ~a~ ~-D ~_ COI~ 00 0~ ~0 O~D r~o .1 ~ Vl Vl _ _ .D O ~ r-~ N ~ _ _ _ ~ _ _ N ~
I.J CJ , o _ _ cv,~ c .
L N O O O V~ O~ CO ~_ 11-1 D ~ O ~ I'_ U7 0 <!:1 V' N U7 N ~ V- ~D O. N _ _I ~ _ ~ N ~ N .
l_ .
. -,0 .V .V .V .V V' V' .V .V.
~ cc. 0 C 0 C~ 0 C~ 0 C~ 0 cV~ 0 C~ 0 C~ 0 ._ ~ L _ 1- ~_ _ l_ ~ _ ~- _ ~- _ l-O ~ _~ L~ ~ L~ _ ~
E o o O o o o o o V L L L L L L L L
0 ~ :~ ~ ~ ~ c~ c a~
7363l.
Example 4 Materials from Heats C, D, E and H having a variety of compositions were processed similar to Heat G in Example 3. Strip materials at a ready-to-finish gage ranging from 0.020-0.060 in. were solution annealed at 1800 F. The annealed strip was finish rolled to effect a reduction of approximately 90%.
Specimens were sectioned in the longitudinal orientation and aged for four hours at 750 F in argon. Tensile properties and electrical conductivity were obtained at room temperature. The results are set forth in Table 6.
.
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aJ o ~ o Lr~ o ~ O ~ o ~ L oc o~ oo ~3'7~
The data of Table 1 show that beryllium-copper alloys containing nickel in excess of trace a~ounts experience an increase in as-annealed hardness with increasing annealing temperature, whereas beryllium copper alloys containina cobalt with only trace amounts of nickel continue to soften with increasing annealing temperature. The reason for this anomalous hardness increase is apparent from Table 2. At annealing temperatures near 1800 F, the nickel-containing beryllium coppers of Table 2 (i.e., Heats A, B and E) form a nickel-rich precipitate which is distinct from both the primary beryllide phase and the principal hardening phase as illustrated in Figures 1 and 2. The cobalt-containing beryllium coppers of Table 2 (i.e., Heats C and D) do not formsuch precipitates at the higher annealing temperature. These nickel-rich precipitates are believed to contribute to the enhanced mechanical and physical -properties of the alloys processed per this invention through: (a) strengtheningof the matrix by dispersion hardening, (b) ductility improvement through inhibition of grain growth at the high annealing temperature and (c) improvementin conductivity through depletion of alloying elements in solid solution.
An additional reason for the improved properties provided in accordance with the invention has to do with the high volume fraction of coherent principalhardening precipitates which forms on aging of material previously subjected to the high solution annealing temperature and substantial cold work. The high solution annealing treatment dissolves more beryllium and nickel plus cobalt in the copper matrix, thereby providing more material available to precipitate on aging. The heavy cold work provides a deformation texture contributing to the high strength.
3~i1 ( Inspection of the data in Tables 4, 5 and 6 indicates that the best combi-nations of strength and ductility resulted from the combination of (a) presence of nickel over a trace amount, (b) annealing temperatures of at least 1800 F and ~c) aging at 750 F. Property combinations including 140,000 psi yield strength, 10% elongation and a conductivity near 50% IACS were obtained. Conductivity and formability were improved by the 8-hour aging time. It is to be appreciated that the alloys tested in Tables 4 and 5 contained less than 0.01% each of iron, cobalt and aluminum and that this low impurity level contributes significantly to electrical conductivity. Nevertheless, strip material of comparable composi-tion conventionally processed by cold rolling even as much as 37% to full hard temper after age hardening to a yield strength of approximately 140,000 psi would be found to have an elongation not exceeding 2%, with poorer formability and lower conductivity. Conversely, material of similar composition subjected to overaging to achieve 60% IACS minimum conductivity would exhibit less than 75,000 psi yield strength.
The data of Table 6 clearly show that cobalt-containing beryllium coppers with only trace amounts of nickel do not respond as favorably to the processing of this invention as do their nickel-containing counterparts.
It is to be further appreciated that the properties reported in Tables 4, 5 and 6 are dependent upon the beryllium and nickel contents of the example heats.
Different chemistries within the ranges defined will yield different property levels, but it is believed that, when processed according to the teachings of the invention, these compositions will yield superior properties compared to the same alloys conventionally processed. Once formed the nickel-rich precipitates described above appear to remain stable and to resist resolution on subsequent reannealing suggesting that additional advantages may accrue from annealing at high temperatures at various process points.
Claims (13)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A thermomechanical process for obtaining improved combinations of properties in beryllium copper alloys consisting essentially of, all by weight, about 1.0% to about 3.5% nickel and cobalt in the aggregate, with at least about 1.0% nickel;
about 0.2% to about 0,7% beryllium; up to about 1.0% zirconium;
up to about 0.005% lead; up to 0.1% magnesium; up to about 1.5%
silver and up to about 0.5% incidental impurities including lead;
and the balance essentially copper, which process comprises the steps of solution treating the alloy at a temperature within about 90% of the incipient melting temperature therefor expressed in degrees Farenheit to effect precipitation of a fine dispersion of a nickel-rich phase, cold working the soltuion treated alloy to reduce the section thickness thereof at least about 60% and thereafter aging the cold worked alloy at a temperature of about 600° to about 900°F. to produce in said alloy in the condition resulting from said aging an improved combination of properties including strength, ductility and electrical conductivity, which on a graph of ultimate tensile strength versus elongation line along or above a line connecting the points defined by 150 ksi ultimate tensile strength at 3.5%
elongation and 120 ksi ultimate tensile strength at 15%
elongation.
about 0.2% to about 0,7% beryllium; up to about 1.0% zirconium;
up to about 0.005% lead; up to 0.1% magnesium; up to about 1.5%
silver and up to about 0.5% incidental impurities including lead;
and the balance essentially copper, which process comprises the steps of solution treating the alloy at a temperature within about 90% of the incipient melting temperature therefor expressed in degrees Farenheit to effect precipitation of a fine dispersion of a nickel-rich phase, cold working the soltuion treated alloy to reduce the section thickness thereof at least about 60% and thereafter aging the cold worked alloy at a temperature of about 600° to about 900°F. to produce in said alloy in the condition resulting from said aging an improved combination of properties including strength, ductility and electrical conductivity, which on a graph of ultimate tensile strength versus elongation line along or above a line connecting the points defined by 150 ksi ultimate tensile strength at 3.5%
elongation and 120 ksi ultimate tensile strength at 15%
elongation.
2. A process in accordance wtih claim 1 which produces in said beryllium copper alloy properties, which on a graph of ultimate tensile strength versus electrical conducitivity, lie along or above a line connecting the points defined by 142 ksi ultimate tensile strength at an electrical conductivity of 42%
IACS and 112 ksi ultimate tensile strength at an electrical conductivity of 61% IACS.
IACS and 112 ksi ultimate tensile strength at an electrical conductivity of 61% IACS.
3. A process in accordance with claim 1 or 2, wherein said beryllium copper alloy contains about 0.4% to about 0.7%
beryllium.
beryllium.
4. A process in accordance with claim 1 or 2, wherein said beryllium copper alloy contains at least about 1.4% nickel.
5. A process in accordance with claim 1 or 2, wherein said beryllium copper alloy contains about 1.8% to about 2.2%
nickel.
nickel.
6. A process in accordance with claim 1 or 2, wherein said solution treatment is conducted at a temperature within about 92% of the incipient melting temperature for the alloy expressed in degrees Fahrenheit.
7. A process in accordance with claim 1 or 2, wherein said solution treatment is conducted at a temperature within about 95% of the incipient melting temperature for the alloy express in degrees Fahrenheit.
8. A process in accordance with claim 1 or 2, wherein said alloy is cold worked to reduce the section thickness thereof at least about 75%.
9. A process in accordance with claim 1 or 2, wherein said alloy is cold worked to reduce the section thickness thereof at least about 80%.
10. A process in accordance with claim 1 or 2, wherein said solution treatment is conducted when said alloy is at a ready-to-finish gage.
11. A process in accordance with claim 1 or 2, wherein said solution treatment is conducted at a temperature of at least about 1800°F.
12. A process in accordance with claim 1 or 2, wherein said alloy is cold worked to reduce the section thickness thereof at least about 90%.
13. Rod, bar, tube, plate, strip and wire made of an age hardenable alloy consisting essentially of at least about 1.0 wt% to about 3.5 wt% nickel and cobalt in the aggregate, with at least about 0.2 wt% to about 0.7 wt% beryllium; up to about 1.0 wt% zirconium; up to about 0,005 wt% lead; up to 0.1 wt%
magnesium; up to about 1.5 wt% silver; and up to about 0.5 wt%
incidental impurities including lead; and the balance essentially copper; having (a) a textured grain orientation, (b) a yield strength higher in the transverse direction than in the longitudinal direction, (c) a microstructure including an optically resolvable nickel-rich phase distinct from the primary beryllide and the principal hardening phases, and (d) an improved combination of properties including strength, ductility and electrical conductivity; which on a graph of ultimate tensile strength versus elongation will lie along or above a line connecting the points defined by 149 ksi ultimate tensile strength at 2% elongation and 100 ksi ultimate tensile strength at 15% elongation.
magnesium; up to about 1.5 wt% silver; and up to about 0.5 wt%
incidental impurities including lead; and the balance essentially copper; having (a) a textured grain orientation, (b) a yield strength higher in the transverse direction than in the longitudinal direction, (c) a microstructure including an optically resolvable nickel-rich phase distinct from the primary beryllide and the principal hardening phases, and (d) an improved combination of properties including strength, ductility and electrical conductivity; which on a graph of ultimate tensile strength versus elongation will lie along or above a line connecting the points defined by 149 ksi ultimate tensile strength at 2% elongation and 100 ksi ultimate tensile strength at 15% elongation.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55063183A | 1983-11-10 | 1983-11-10 | |
| US550,631 | 1983-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1237361A true CA1237361A (en) | 1988-05-31 |
Family
ID=24197967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000465690A Expired CA1237361A (en) | 1983-11-10 | 1984-10-17 | Thermomechanical processing of beryllium-copper alloys |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPH0826442B2 (en) |
| CA (1) | CA1237361A (en) |
| CH (1) | CH662822A5 (en) |
| DE (1) | DE3439721C2 (en) |
| FR (1) | FR2554830B1 (en) |
| GB (1) | GB2149819B (en) |
| IT (1) | IT1198957B (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4565586A (en) * | 1984-06-22 | 1986-01-21 | Brush Wellman Inc. | Processing of copper alloys |
| US4599120A (en) * | 1985-02-25 | 1986-07-08 | Brush Wellman Inc. | Processing of copper alloys |
| DE3773470D1 (en) * | 1986-11-13 | 1991-11-07 | Ngk Insulators Ltd | PRODUCTION OF COPPER-BERYLLIUM ALLOYS. |
| JPS63223151A (en) * | 1987-03-12 | 1988-09-16 | Ngk Insulators Ltd | Formed body for parts composed of berylium-copper alloy material and its production |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE539762C (en) * | 1926-10-20 | 1931-12-02 | Ver Deutsche Metallwerke Akt G | Compensation for copper-beryllium alloys |
| GB534288A (en) * | 1938-10-21 | 1941-03-04 | Westinghouse Electric Int Co | Improvements in or relating to copper base alloys |
| GB952545A (en) * | 1961-04-20 | 1964-03-18 | Westinghouse Electric Corp | Improved copper base alloys |
| US3663311A (en) * | 1969-05-21 | 1972-05-16 | Bell Telephone Labor Inc | Processing of copper alloys |
| JPS5949294B2 (en) * | 1977-03-14 | 1984-12-01 | 株式会社東芝 | Copper alloy and its manufacturing method |
| US4179314A (en) * | 1978-12-11 | 1979-12-18 | Kawecki Berylco Industries, Inc. | Treatment of beryllium-copper alloy and articles made therefrom |
-
1984
- 1984-10-17 CA CA000465690A patent/CA1237361A/en not_active Expired
- 1984-10-30 DE DE3439721A patent/DE3439721C2/en not_active Expired - Fee Related
- 1984-11-01 GB GB08427628A patent/GB2149819B/en not_active Expired
- 1984-11-09 IT IT09532/84A patent/IT1198957B/en active
- 1984-11-09 JP JP59235314A patent/JPH0826442B2/en not_active Expired - Lifetime
- 1984-11-09 FR FR848417127A patent/FR2554830B1/en not_active Expired - Fee Related
- 1984-11-09 CH CH5379/84A patent/CH662822A5/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60169535A (en) | 1985-09-03 |
| DE3439721C2 (en) | 1995-06-08 |
| JPH0826442B2 (en) | 1996-03-13 |
| FR2554830B1 (en) | 1992-09-11 |
| DE3439721A1 (en) | 1985-05-23 |
| FR2554830A1 (en) | 1985-05-17 |
| GB2149819A (en) | 1985-06-19 |
| IT1198957B (en) | 1988-12-21 |
| GB8427628D0 (en) | 1984-12-05 |
| CH662822A5 (en) | 1987-10-30 |
| GB2149819B (en) | 1987-05-13 |
| IT8409532A0 (en) | 1984-11-09 |
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