US3772092A - Copper base alloys - Google Patents
Copper base alloys Download PDFInfo
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- US3772092A US3772092A US00196002A US3772092DA US3772092A US 3772092 A US3772092 A US 3772092A US 00196002 A US00196002 A US 00196002A US 3772092D A US3772092D A US 3772092DA US 3772092 A US3772092 A US 3772092A
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/06—Alloys based on copper with nickel or cobalt as the next major constituent
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/05—Alloys based on copper with manganese as the next major constituent
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- Copper base alloys which contain relatively large amounts of nickel and manganese. Alloys of this type are highly desirable since they are capable of obtaining yield strengths in excess of 200 ksi upon aging. In addition, these alloys appear to have reasonable processing and in particular are not quench sensitive.
- the alloy of the present invention consists essentially of from 12.5 to 30 percent nickel, from 12.5 to 30 percent manganese, from 0.1 to 3.5 percent zinc and a material selected from the group consisting of aluminum from 0.01 to 5 percent, magnesium from 0.01 to 5 percent, boron from 0.001 to 0.1 percent mixtures thereof, balance essentially copper, wherein the nickel to manganese ratio is at least 0.75 and preferably 1.0 or higher.
- FIG. 1 is a graph plotting the fracture toughness as a function of yield strength for various alloys, representing the properties longitudinal to the rolling direction;
- FIG. 2 is a similar graph plotting the fracture toughness as a function of yield strength for various alloys, representing the properties transverse to the rolling direction.
- the foregoing alloy has been found to obtain surprisingly improved fracture toughness while retaining the excellent strength characteristics of this alloy system.
- the alloy of the present invention is an excellent lower priced replacement for beryllium-copper, with increased fracture toughness.
- the alloy of the present invention achieves levels of fracture toughness approaching high alloy steels which are limited in applicability by poor corrosion resistance.
- the alloys of the present invention are superior to maraging steels in marine environments since the alloys of the present invention are not susceptible to hydrogen embrittlement.
- the alloys of the present invention are characterized by excellent stress corrosion resistance.
- the instant alloys contain from 12.5 to 30 percent nickel, and from 12.5 to 30 percent manganese.
- both the nickel and manganese contents should range from 15 to 25 percent.
- the nickel to manganese ratio must be at least 0.75 and preferably 1.0 or higher.
- the nickel and manganese contents have an affect on aging response, yield strength and workability of the alloys.
- increasing the amount of nickel and manganese has deleterious effects on the workability of the alloys during processing, especially over 30 percent each of nickel and manganese.
- the preferred nickel to manganese ratio is 1.0 or higher.
- the maximum aging response is obtained for a given amount of nickel and manganese when the nickel to manganese ratio is about 1.0. If the ratio is less than 1.0, an excess of manganese exists which can have adverse effects on the stress corrosion resistance of the alloy. A ratio greater than about 1.5 does not give improved results over a ratio of about 1.0 and is more expensive due to the high cost of the nickel.
- the alloy of the present invention contains a material selected frbm the group consisting of aluminum in an amount from 0.01 to 5.0 percent, magnesium from 0.01 to 5.0 percent, boron from 0.001 to 0.1 percent and mixtures thereof.
- Aluminum is the preferred addition since it tends to form a protective oxide coating during melting.
- the aluminum should be added in an amount from 0.01 to 0.75 percent.
- magnesium should be used in an amount from 0.01 to 0.75 percent as a deoxidant.
- the aluminum and magnesium may be used as advantageous alloying additions in amounts greater than 0.6 percent for increased corrosion resistance and fracture toughness. The aluminum when used at the higher levels, also tends to modify the cellular precipitate at the grain boundaries.
- the zinc component should be present in an amount from 0.1 to 3.5 percent. Increased amounts of zinc over 3.5 percent give rise to a decrease in the stress corrosion resistance and fracture toughness.
- the zinc addition controls the grain size, reduces the cellular precipitate at the grain boundaries, changes the morphology of the inclusions, promotes sound castings and increases the aging response of the alloy. It is most surprising that so many advantages may be realized from a single alloying addition.
- the grain size control may be attributed to a fine dispersoid which is present in the zinc containing alloys.
- the increased aging respouse is due to an increase in the growth rate of the precipitate.
- the preferred zinc content is from 1 to 3 percent.
- Tin is a particularly desirable additive in an amount from 0.01 to 2 percent and preferably from 0.5 to 1.0 percent. Tin tends to alter the morphology of the cellular precipitate at the grain boundary.
- Zirconium and/or titanium are preferred alloying additions in amounts 0.01 to 2.0 percent each, and preferably from 0.15 to 0.30 percent each. These materials tend to desirably change morphology and chemistry of inclusions and desirably change morphology of cellular precipitate at grain boundaries.
- chromium is a desirable addition in an amount from 0.01 to 1.0 percent, and preferably from 0.15 to 0.30 percent. Chromium tends to control the grain size and change the morphology and chemistry of inclusions.
- Additional desirable alloying additoins are cobalt and/or iron in amounts from 0.05 to 1.0 percent each, and preferably from 0.2 to 0.5 percent each. These materials also tend to control the grain size.
- the casting of the alloy of the present invention is not particularly significant. Any convenient method of casting may be employed. Pouring temperatures in the range of about 1,000 to 1,200C. are preferably employed, with an optimum pouring temperature in the range of l,050 to 1,100C.
- the alloy of the present invention is processed by breakdown of ingot into strip using a hot rolling operation followed by cold rolling and annealing cycles to reach final gage.
- Preferred properties are obtained using an aging treatment.
- the starting hot rolling temperature be in the range of 700 to 900C, and preferably 780 to 900Cv
- the cooling rate from hot rolling should preferably be in excess of 25C. per hour down to 300C. in order to avoid precipitation of manganesenickel rich phases.
- the alloy is capable of cold rolling reductions in excess of 90 percent, but the cold rolling reduction should preferably be between 30 and 80 percent in order to control the grain size.
- an average grain size less than 0.015 mm gives the optimum fracture toughness.
- An average grain size of this order can be obtained by control of the cold rolling reduction, annealing times and annealing temperatures. In general, annealing temperatures in the range of 550 to 900C. for times from one minute to 10 hours can give the required grain size.
- the material After annealing, the material is cooled in excess of 25C. per hour down to 300C., as indicated above, and the cold rolling and annealing cycles repeated as desired depending on gage requirements.
- the alloy of the present invention may be aged in the range of 250 to 475C, with temperatures of 380 to 460C. being preferred. Aging times of 30 minutes to 10 hours, with preferred times of 1 to 6 hours, are used to obtain the desired properties.
- controlling the amount of cold work prior to aging has an effect on fracture toughness and aging response.
- the cold work gives rise to increased nucleation sites for the intragranular precipitation of the discrete manganese-nickel rich particles.
- cold working of the alloys prior to aging at the higher temperatures of the aging range increases the aging response and decreases the amount of cellular precipitate.
- the amount of cold rolling can vary from 10 to 50 percent, with from 15 to 45 percent yielding the optimum fracture toughness.
- EXAMPLE I The Durville method was used to cast the various alloys listed in Table I. The copper and nickel were melted under a charcoal cover. Aluminum was added to deoxidize the melt. Following the removal of the charcoal cover, the manganese and zinc additions were made. The slag was removed and the melt was poured from approximately 1080C.
- Tables 2A and 2B represent the properties longitudinal to the rolling direction and Table 2B represents the properties transverse to the rolling direction, with a copper-2 percent beryllium alloy shown for comparison.
- UPE is a relative value of the fracture toughness determined by the Kahn Tear Test.
- the alloys were annealed at different temperatures to control the grain size. Therefore, the effect of the various zinc additions could be determined independent of any effect of grain size on the alloys.
- the average grain size of the alloys tested was 0.005 to 0.010 mm.
- the fracture toughness is plotted as a function Alloy Aging Time at Yield Strength UPE 450C, Hours 0.2% Offset in.lb./in
- a wrought copper base alloy having improved toughness and stress corrosion resistance consisting essentially of from 12.5 to 30 percent nickel, from 12.5 to 30 percent manganese, from 0.1 to 3.5 percent zinc, and a material selected from the group consisting of aluminum from 0.01 to 5 percent, magnesium from 0.01 to 5 percent, boron from 0.001 to 0.1 percent and mixtures thereof, balance essentially copper, wherein the nickel to manganese ratio is from 0.75 to 1.5, said alloy having an average grain size less than 0.015 mm. and an intragranular precipitation of discrete manganese-nickel rich particles.
- An alloy according to claim 1 containing a material selected from the group consisting of iron from 0.05 to 1 percent, cobalt from 0.05 to 1 percent mixtures thereof.
Abstract
The disclosure teaches novel copper base alloys having improved toughness and stress corrosion resistance. The copper alloys contain from 12.5 to 30 percent nickel, from 12.5 to 30 percent manganese, a material selected from the group consisting of aluminum from 0.01 to 5 percent, boron from 0.001 to 0.1 percent, magnesium from 0.01 to 5 percent and mixtures thereof and zinc from 0.1 to 3.5 percent.
Description
United States Patent [191 Shapiro et a1.
[ COPPER BASE ALLOYS [75] Inventors: Stanley Shapiro, New Haven, Conn;
Alan J. Goldman, Silver Springs, Md.; Derek E. Tyler, Cheshire; Richard D. Lanam, Hamden, both of Conn.
[73] Assignee: Olin Corporation, New Haven,
Conn.
[22] Filed: Nov. 5, 1971 21 Appl. No.: 196,002
[52] U.S. Cl 148/325, 75/153, 75/157.5, 75/159, 75/161, 75/162,148/l2.7,148/32,148/l60 [51] Int. Cl C22c 9/04, C22f 1/08 [58] Field of Search 75/153, 157, 157.5, 75/15 9,l61,162,164;148/12.7, 32.5,160
[56] References Cited UNITED STATES PATENTS 2,234,552 3/1941 Dean et a1. 75/159 X FOREIGN PATENTS OR APPLICATIONS 1,092,218 11/1960 Germany 75/159 Nov. 13, 1973 578,223 6/1906 Great Britain 75/159 24,220 10/1964 Japan 75/159 577,170 5/1946 Great Britain.. 75/159 577,597 5/1946 Great Britain 75/159 719,979 4/1942 Germany 75/159 OTHER PUBLICATIONS Electrolytic Manganese and Its Alloys, Dean The Ronald Press Co. 1952 NY. pgs 146,147, 188-191 Primary Examiner-Char1es N. Lovell Attorney-Robert H. Bachman et a1.
[57] ABSTRACT 8 Claims, 2 Drawing Figures PATENTEURM 1 3 I973 UPE. m. /b,//I7.
SHEET F 2 I I I I I u m ALLOY A o ALLOY a ALLOY c aooq- A ALLOY 0 ALLOY E cw) O O I I T --4- 150 I I I 200 2/0 0.2% OFFSET V/ELO STRENGTH (KSO LONG/TUD/NAL PROPERTIES INVENTORS STANLEY SHAP/RO ALAN J. GOLDMAN DEREK E. TYLER RICHARD D. LANAM ATTORNEY UPE m. lb. 1/1
PAIENIEBIUV 13' ms 3. 7 72.092 SHEET 2 BF 2 [1 ALLOY A ALL 300-- 0 0y ALLOY c A ALLOY 0 Q ALLOY E cw) o A 0 l I O INVENTORS.
STANLEY SHAP/RO ALAN J GOLDMAN DEREK E. TYLER RICHARD D. LANAM I BYWM ATTORNEY 1 COPPER BASE ALLOYS BACKGROUND OF THE INVENTION Copper base alloys are known which contain relatively large amounts of nickel and manganese. Alloys of this type are highly desirable since they are capable of obtaining yield strengths in excess of 200 ksi upon aging. In addition, these alloys appear to have reasonable processing and in particular are not quench sensitive.
The presence of a marked aging response to obtain high strengths in eopper-nickel-manganese alloys is known. It has been found that different types of precipitation reactions may occur in this alloy system, depending on the aging temperature. For example, aging at a low temperature, such as 350C, yields a cellular precipitate which nucleates at the grain boundaries and with time grows throughout the entire grain. The cellular precipitate consists of adjacent lamellae of a manganese-nickel rich phase and the copper-rich solid solution. Aging at higher temperatures, such as 450C., yields mainly finely dispersed, spherical precipitates of the manganese-nickel rich phase within the grains and only a small amount of the cellular precipitate at the grain boundaries.
However, in any event, the presence of a cellular precipitate at grain boundaries is generally found to have deleterious effects on alloy properties, such as fracture toughness and stress corrosion resistance. This is indeed found to bethe case in these alloys and is a significant factor in the limited commercial success which these alloys have enjoyed. I
It would be highly desirable to develop an alloy within the copper-manganese-nickel alloy system which has increased fracture toughness. It would also be highly desirable to improve the stress corrosion resistance of such alloys.
Accordingly, it is a principal object of the present invention to develop a copper base alloy containing relatively large amounts of nickel and manganese.
It is an additional object of the present invention to develop an alloy as aforesaid which is capable of obtaining yield strengths in excess of 200 ksi upon aging.
It is a still further object of the present invention to develop an alloy as aforesaid which is readily processed commercially and which is characterized by improved fracture toughness.
It is a still further object of the present invention to provide a copper base alloy with good stress corrosion resistance, good ductility, toughness and excellent yield strength characteristics.
Further objects and advantages of the present invention will appear from the ensuing discussion.
SUMMARY OF THE INVENTION In accordance with the present invention, it has now been found that the foregoing objects and advantages may be readily obtained.
The alloy of the present invention consists essentially of from 12.5 to 30 percent nickel, from 12.5 to 30 percent manganese, from 0.1 to 3.5 percent zinc and a material selected from the group consisting of aluminum from 0.01 to 5 percent, magnesium from 0.01 to 5 percent, boron from 0.001 to 0.1 percent mixtures thereof, balance essentially copper, wherein the nickel to manganese ratio is at least 0.75 and preferably 1.0 or higher.
BRIEF DESCRIPTION OF DRAWINGS In the drawings which form a part of the present specification:
FIG. 1 is a graph plotting the fracture toughness as a function of yield strength for various alloys, representing the properties longitudinal to the rolling direction; and
FIG. 2 is a similar graph plotting the fracture toughness as a function of yield strength for various alloys, representing the properties transverse to the rolling direction.
DETAILED DESCRIPTION In accordance with the present invention, the foregoing alloy has been found to obtain surprisingly improved fracture toughness while retaining the excellent strength characteristics of this alloy system.
This enables the attainment of several significant advantages. The alloy of the present invention is an excellent lower priced replacement for beryllium-copper, with increased fracture toughness. The alloy of the present invention achieves levels of fracture toughness approaching high alloy steels which are limited in applicability by poor corrosion resistance. The alloys of the present invention are superior to maraging steels in marine environments since the alloys of the present invention are not susceptible to hydrogen embrittlement. In addition, the alloys of the present invention are characterized by excellent stress corrosion resistance.
In accordance with the present invention, the instant alloys contain from 12.5 to 30 percent nickel, and from 12.5 to 30 percent manganese. Preferably, both the nickel and manganese contents should range from 15 to 25 percent. The nickel to manganese ratio must be at least 0.75 and preferably 1.0 or higher.
The nickel and manganese contents have an affect on aging response, yield strength and workability of the alloys. The lower the manganese and nickel content, the slower the aging response and lower the maximum yield strength obtainable upon aging, especially below 12.5 percent nickel and manganese. On the other hand, increasing the amount of nickel and manganese has deleterious effects on the workability of the alloys during processing, especially over 30 percent each of nickel and manganese.
As indicated hereinabove, the preferred nickel to manganese ratio is 1.0 or higher. The maximum aging response is obtained for a given amount of nickel and manganese when the nickel to manganese ratio is about 1.0. If the ratio is less than 1.0, an excess of manganese exists which can have adverse effects on the stress corrosion resistance of the alloy. A ratio greater than about 1.5 does not give improved results over a ratio of about 1.0 and is more expensive due to the high cost of the nickel.
In addition to the foregoing, the alloy of the present invention contains a material selected frbm the group consisting of aluminum in an amount from 0.01 to 5.0 percent, magnesium from 0.01 to 5.0 percent, boron from 0.001 to 0.1 percent and mixtures thereof. Each of these elements act as deoxidizers and assist in the melting of the alloys. Aluminum is the preferred addition since it tends to form a protective oxide coating during melting. When aluminum is used as a deoxidant only, the aluminum should be added in an amount from 0.01 to 0.75 percent. Similarly, magnesium should be used in an amount from 0.01 to 0.75 percent as a deoxidant. In addition, the aluminum and magnesium may be used as advantageous alloying additions in amounts greater than 0.6 percent for increased corrosion resistance and fracture toughness. The aluminum when used at the higher levels, also tends to modify the cellular precipitate at the grain boundaries.
The zinc component should be present in an amount from 0.1 to 3.5 percent. Increased amounts of zinc over 3.5 percent give rise to a decrease in the stress corrosion resistance and fracture toughness.
The zinc addition controls the grain size, reduces the cellular precipitate at the grain boundaries, changes the morphology of the inclusions, promotes sound castings and increases the aging response of the alloy. It is most surprising that so many advantages may be realized from a single alloying addition. The grain size control may be attributed to a fine dispersoid which is present in the zinc containing alloys. The increased aging respouse is due to an increase in the growth rate of the precipitate. The preferred zinc content is from 1 to 3 percent.
In addition to the foregoing, several additives are particularly advantageous. Tin is a particularly desirable additive in an amount from 0.01 to 2 percent and preferably from 0.5 to 1.0 percent. Tin tends to alter the morphology of the cellular precipitate at the grain boundary.
Zirconium and/or titanium are preferred alloying additions in amounts 0.01 to 2.0 percent each, and preferably from 0.15 to 0.30 percent each. These materials tend to desirably change morphology and chemistry of inclusions and desirably change morphology of cellular precipitate at grain boundaries.
In addition, chromium is a desirable addition in an amount from 0.01 to 1.0 percent, and preferably from 0.15 to 0.30 percent. Chromium tends to control the grain size and change the morphology and chemistry of inclusions.
Additional desirable alloying additoins are cobalt and/or iron in amounts from 0.05 to 1.0 percent each, and preferably from 0.2 to 0.5 percent each. These materials also tend to control the grain size.
Naturally, other additives may be desirable in order to achieve or accentuate a particular property and conventional impurities may be tolerated.
The casting of the alloy of the present invention is not particularly significant. Any convenient method of casting may be employed. Pouring temperatures in the range of about 1,000 to 1,200C. are preferably employed, with an optimum pouring temperature in the range of l,050 to 1,100C.
Generally, the alloy of the present invention is processed by breakdown of ingot into strip using a hot rolling operation followed by cold rolling and annealing cycles to reach final gage. Preferred properties are obtained using an aging treatment.
It is preferred that the starting hot rolling temperature be in the range of 700 to 900C, and preferably 780 to 900Cv The cooling rate from hot rolling should preferably be in excess of 25C. per hour down to 300C. in order to avoid precipitation of manganesenickel rich phases. The alloy is capable of cold rolling reductions in excess of 90 percent, but the cold rolling reduction should preferably be between 30 and 80 percent in order to control the grain size.
It has been found that an average grain size less than 0.015 mm gives the optimum fracture toughness. An average grain size of this order can be obtained by control of the cold rolling reduction, annealing times and annealing temperatures. In general, annealing temperatures in the range of 550 to 900C. for times from one minute to 10 hours can give the required grain size.
After annealing, the material is cooled in excess of 25C. per hour down to 300C., as indicated above, and the cold rolling and annealing cycles repeated as desired depending on gage requirements.
The alloy of the present invention, as previously stated, may be aged in the range of 250 to 475C, with temperatures of 380 to 460C. being preferred. Aging times of 30 minutes to 10 hours, with preferred times of 1 to 6 hours, are used to obtain the desired properties. In addition, it has been found that controlling the amount of cold work prior to aging has an effect on fracture toughness and aging response. In particular, it has been observed that the cold work gives rise to increased nucleation sites for the intragranular precipitation of the discrete manganese-nickel rich particles. Hence, cold working of the alloys prior to aging at the higher temperatures of the aging range increases the aging response and decreases the amount of cellular precipitate. The amount of cold rolling can vary from 10 to 50 percent, with from 15 to 45 percent yielding the optimum fracture toughness.
The present invention will be more readily understandable from a consideration of the following illustrative examples.
EXAMPLE I The Durville method was used to cast the various alloys listed in Table I. The copper and nickel were melted under a charcoal cover. Aluminum was added to deoxidize the melt. Following the removal of the charcoal cover, the manganese and zinc additions were made. The slag was removed and the melt was poured from approximately 1080C.
TABLE 1 Composition Weight Alloy Nickel Manganese Aluminum Zinc Copper A 19.72 19.92 .36 Substantially balance B 20.01 19.80 .39 2.17 Substantially balance C 19.72 19.78 .39 4,25 Substantially balance D 19.89 19.50 .40 6.34 Substantially balance EXAMPLE II The alloys prepared in Example I were processed in the following manner. All alloys were homogenized at 840C. for about 2 hours. The materials were hot rolled from 1.500 inches to 0.418 inches and water quenched. The alloys were cold rolled 60 percent to 0.16) inches. Alloys A, B and C were annealed at 600C. for about 30 minutes and Alloy D was annealed at 625C. for about 30 minutes. After a water quench, the alloys were cold rolled 60 percent to 0.067 inch and annealed and quenched again in the same manner. Subsequent to the water quench, the alloys were cold rolled 25 percent to 0.050 inches and aged at 450C. for various times. The resultant properties were determined after various aging times. These are indicated in Tables 2A and 2B below. Table 2A represents the properties longitudinal to the rolling direction and Table 2B represents the properties transverse to the rolling direction, with a copper-2 percent beryllium alloy shown for comparison. The term UPE is a relative value of the fracture toughness determined by the Kahn Tear Test.
The alloys were annealed at different temperatures to control the grain size. Therefore, the effect of the various zinc additions could be determined independent of any effect of grain size on the alloys. The average grain size of the alloys tested was 0.005 to 0.010 mm.
TABLE 2A Longitudinal Properties The data are presented in graphical form in FIGS. 1
and 2. The fracture toughness is plotted as a function Alloy Aging Time at Yield Strength UPE 450C, Hours 0.2% Offset in.lb./in
ksi A 2.5 170 375 A 3.0 178 220 A 3.5 184 1 19 B 2.0 187 212 B 3.5 204 15 C 1.0 176 80 C 2.0 195 8 C 3.0 208 0 D 1.5 159 207 D 2.0 175 153 D 2.5 182 31 Aged 316C.
Cu/ZBe 1.5 165 42 Cu/2Be 2.0 175 18 TAB LE 28 Transverse Properties Alloy Aging Time at Yield Strength UPE 450C, Hours 0.2% Offset 1n.lb./in.
ksi
A 2.5 150 172 A 3.0 161 80 A 3.5 163 25 B 1.0 144 330 B 2.0 173 150 B 3.5 204 0 C 1.0 154 42 C 2.0 183 0 C 3.0 196 0 D 1.5 157 51 D 2.0 168 15 D 2.5 174 15 Aged 316C. Cu/ZBe 1.5 171 5 Cu/2Be 2.0 173 0 Cu/2Be 2.5 178 0 carried out in other ways without departing from the -spirit or essential characteristics thereof. The present embodiment is therefore to be considered as in all rejspects illustrative and not restrictive, the scope of the invention being indicated by the appended claims, and all changes which come within the meaning and range of equivalency are intended to be embraced therein.
What is claimed is:
l. A wrought copper base alloy having improved toughness and stress corrosion resistance consisting essentially of from 12.5 to 30 percent nickel, from 12.5 to 30 percent manganese, from 0.1 to 3.5 percent zinc, and a material selected from the group consisting of aluminum from 0.01 to 5 percent, magnesium from 0.01 to 5 percent, boron from 0.001 to 0.1 percent and mixtures thereof, balance essentially copper, wherein the nickel to manganese ratio is from 0.75 to 1.5, said alloy having an average grain size less than 0.015 mm. and an intragranular precipitation of discrete manganese-nickel rich particles.
2. An alloy according to claim 1 wherein the nickel content is from 15 to 25 percent and the manganese content is from 15 to 25 percent.
3. An alloy according to claim 1 wherein said material is aluminum in an amount from 0.6 to 5 percent.
4. An alloy according to claim 1 wherein said material is magnesium in an amount from 0.6 to 5 percent.
5. An alloy according to claim 1 wherein said material is aluminum in an amount from 0.01 to 0.75 percent.
6. An alloy according to claim 1 wherein said material is magnesium in an amount from 0.01 to 0.75 percent.
7. An alloy according to claim 1 wherein the zinc content is from 1 to 3 percent.
8. An alloy according to claim 1 containing a material selected from the group consisting of iron from 0.05 to 1 percent, cobalt from 0.05 to 1 percent mixtures thereof.
Claims (7)
- 2. An alloy according to claim 1 wherein the nickel content is from 15 to 25 percent and the manganese content is from 15 to 25 percent.
- 3. An alloy according to claim 1 wherein said material is aluminum in an amount from 0.6 to 5 percent.
- 4. An alloy according to claim 1 wherein said material is magnesium in an amount from 0.6 to 5 percent.
- 5. An alloy according to claim 1 wherein said material is aluminum in an amount from 0.01 to 0.75 percent.
- 6. An alloy according to claim 1 wherein said material is magnesium in an amount from 0.01 to 0.75 percent.
- 7. An alloy according to claim 1 wherein the zinc content is from 1 to 3 percent.
- 8. An alloy according to claim 1 containing a material selected from the group consisting of iron from 0.05 to 1 percent, cobalt from 0.05 to 1 percent mixtures thereof.
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US19600271A | 1971-11-05 | 1971-11-05 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US4337793A (en) * | 1974-12-23 | 1982-07-06 | Sumitomo Light Metal Industries, Ltd. | Copper-alloy tube water supply |
US4434016A (en) | 1983-02-18 | 1984-02-28 | Olin Corporation | Precipitation hardenable copper alloy and process |
WO1994001591A1 (en) * | 1992-07-01 | 1994-01-20 | Olin Corporation | Machinable copper alloys having reduced lead content |
US11123825B2 (en) * | 2016-08-31 | 2021-09-21 | Faurecia Emissions Control Technologies, Germany Gmbh | Copper-based brazing material and use of the brazing material |
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GB577170A (en) * | 1941-04-21 | 1946-05-08 | Maurice Cook | Improvements in or relating to hard copper alloys |
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DE719979C (en) * | 1939-07-27 | 1942-04-21 | Heraeus Vacuumschmelze Ag | Manganese alloys with a high expansion coefficient |
US2234552A (en) * | 1939-10-23 | 1941-03-11 | Chicago Dev Co | Hardened nonferrous alloy |
GB577170A (en) * | 1941-04-21 | 1946-05-08 | Maurice Cook | Improvements in or relating to hard copper alloys |
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Cited By (5)
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US4337793A (en) * | 1974-12-23 | 1982-07-06 | Sumitomo Light Metal Industries, Ltd. | Copper-alloy tube water supply |
US4434016A (en) | 1983-02-18 | 1984-02-28 | Olin Corporation | Precipitation hardenable copper alloy and process |
US5409552A (en) * | 1991-03-01 | 1995-04-25 | Olin Corporation | Machinable copper alloys having reduced lead content |
WO1994001591A1 (en) * | 1992-07-01 | 1994-01-20 | Olin Corporation | Machinable copper alloys having reduced lead content |
US11123825B2 (en) * | 2016-08-31 | 2021-09-21 | Faurecia Emissions Control Technologies, Germany Gmbh | Copper-based brazing material and use of the brazing material |
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