US2247643A - Hardening cobalt-nickel-chromium-iron alloys - Google Patents
Hardening cobalt-nickel-chromium-iron alloys Download PDFInfo
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- US2247643A US2247643A US362236A US36223640A US2247643A US 2247643 A US2247643 A US 2247643A US 362236 A US362236 A US 362236A US 36223640 A US36223640 A US 36223640A US 2247643 A US2247643 A US 2247643A
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/03—Alloys based on nickel or cobalt based on nickel
- C22C19/05—Alloys based on nickel or cobalt based on nickel with chromium
- C22C19/051—Alloys based on nickel or cobalt based on nickel with chromium and Mo or W
- C22C19/055—Alloys based on nickel or cobalt based on nickel with chromium and Mo or W with the maximum Cr content being at least 20% but less than 30%
Definitions
- This invention relates to a method of hardening certain cobalt-nickel-chromium-iron alloys having improved mechanical properties at elevated temperatures.
- alloys which in addition to nickel as main constituent contain alternatively proportions of chromium, molybdenum or tungsten as well as on accasion iron, show a high creep resistance in hard rolled condition at operating temperatures between about 400 and 600 C.
- the alloys according to this invention contain as main constituents cobalt and nickel in a total quantity of 50 to 70% the cobalt content amounting to at least 10% and the nickel content amounting to at least 0.05%.
- Tungsten and molybdenum may be present separately or together in amounts of from 0.05% up to 20%, for example from 2.5 to 15%, and the chromium content amounts to between 8 and 25%.
- the alloys may contain up to 30% of iron, for instance, from 0.5 to 30% of iron.
- a particularly good composition is 14 to 17% chromium, 14 to 16% iron, 5 to 7% molybdenum, to.
- the alloys are to be used at temperatures above their recrystallisation temperatures, the highest creep resistance is exhibited by the alloys stated when they have been annealed prior to their use at temperatures exceeding the temperatures of use, for example at 1150 to 1300 C. If desired the alloys can also be employed in cast condition.
- the creep resistance may be increased by forging, rolling, drawing or hammering at the temperature between the tempera ture at which the alloys are to be used, and the recrystallisation temperature. method not only the creep resistance but especially the elongation under the first loading ot'thc material is decreased.
- the advance over the known alloys is clear it the creep limit as such is not taken for comparison, but creep with time'which is frequently adopted for comparison, that is to say the elongation per unit of time which a test piece undergoes when loaded with a given weight at constant temperature for a long time.
- a comparative investigation about the creep resistance shows that the rate of creep of the cobalt-containing alloys according to the invention at constant temperature under a given load is only about one fifth to one tenth as compared with the abovementioned alloys of known composition.
- the stem may be provided with a thin hardened surface layer by hammering, pressing, pressure polishing or pressure rolling and thus valuable running properties under conditions of deficient lubrication obtained.
- the alloys so modified can be subjected tostill higher mechanical load at high temperatures, that is to say the mechanical properties at a given temperature are better than those of the alloys without .the apeciiied additions, or the temperature at "which the alloys can stand a predetermined mechanical load may be higher.
- a particularly advantageous alloy can be obtained with about 15 to 27% cobalt, 14 to 17% chromium, 6 to 16% iron, 5 to 7% molybdenum, 0 to 7% tungsten, especially 3 to 7% tungsten, besides nickels also main constituents, with additions of up to 5% titanium, up to 15% tantalum, up to 15% columbium, up to 8% thorium, and possibly the usual deoxidising and manuiacturing additions.
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- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
Description
Patented July 1, 1941 HABDENING COBALT-NICKEL-EHRQMEUM- IRON ALLOYS Wilhelm Rohn, Hanan on the Main, Franz Bollenrath, Berlin-Johannisthal, and Heinrich Cornelius, Berlln-Adlershot, Germany No Drawing. Original application December 24,
1938, Serial No. 247,696.
Divided and this application October 22, 1940, Serial No. 362,236. In Germany April v24, 1936 1 Claim. ((21.148-4) This application is a division of our copending patent application Ser. No. 247,696, filed Dec. 24, 1938.
This invention relates to a method of hardening certain cobalt-nickel-chromium-iron alloys having improved mechanical properties at elevated temperatures.
It is known that alloys which in addition to nickel as main constituent contain alternatively proportions of chromium, molybdenum or tungsten as well as on accasion iron, show a high creep resistance in hard rolled condition at operating temperatures between about 400 and 600 C.
Investigations by the applicants have now led to the development of alloys which on the one hand exhibit particularly high values of creep resistance at temperatures between 400 and 600 C. and which probably in this range show the optimum with regard to strength at high temperatures and which on the other hand still show also a high creep resistance at higher temperatures that is to say at temperatures up to and above 900 C. Consequently they are for example suitable for the exhaust valves of internal combustion engines and exhaust turbines which operate in the temperature range of 600 to 900 C.
The alloys according to this invention contain as main constituents cobalt and nickel in a total quantity of 50 to 70% the cobalt content amounting to at least 10% and the nickel content amounting to at least 0.05%. Tungsten and molybdenum may be present separately or together in amounts of from 0.05% up to 20%, for example from 2.5 to 15%, and the chromium content amounts to between 8 and 25%. In addition the alloys may contain up to 30% of iron, for instance, from 0.5 to 30% of iron. A particularly good composition is 14 to 17% chromium, 14 to 16% iron, 5 to 7% molybdenum, to. tungsten, to 27% (particularly 21%) of cobalt, and the remainder essentially nickel apart from the usual deoxidising and manufacturing additions, for example of manganese and silicon. The manganese content may for example amount up to 1.5% and the silicon content up to 0.5%. If the alloys are to be used at temperatures above their recrystallisation temperatures, the highest creep resistance is exhibited by the alloys stated when they have been annealed prior to their use at temperatures exceeding the temperatures of use, for example at 1150 to 1300 C. If desired the alloys can also be employed in cast condition. If the alloys are to be used at temperatures below their recrystallisation temperatures the creep resistance may be increased by forging, rolling, drawing or hammering at the temperature between the tempera ture at which the alloys are to be used, and the recrystallisation temperature. method not only the creep resistance but especially the elongation under the first loading ot'thc material is decreased.
An alloy with about 16% chromium, about 15% iron, about 6% molybdenum, about 40% nickel and about 21% cobalt besides small proportions of de-oxidising and manufacturing additions exceeds by about 10 to 15% as regards creep resistance in the temperature range 500 to 600 C, an alloy hitherto considered as particularly' good in this respect and consisting of 60% nickel, 15% chromium, 7% molybdenum and 18% iron. The advance over the known alloys is clear it the creep limit as such is not taken for comparison, but creep with time'which is frequently adopted for comparison, that is to say the elongation per unit of time which a test piece undergoes when loaded with a given weight at constant temperature for a long time.-
A comparative investigation about the creep resistance shows that the rate of creep of the cobalt-containing alloys according to the invention at constant temperature under a given load is only about one fifth to one tenth as compared with the abovementioned alloys of known composition.
As a result of the considerable hardening which can be effected by cold working the stem may be provided with a thin hardened surface layer by hammering, pressing, pressure polishing or pressure rolling and thus valuable running properties under conditions of deficient lubrication obtained.
A further improvement, in particular as regards the resistance to creep at high temperatures, can be attained with the said alloys ii an addition is made of one or more of the elements By this special.
thorium) or of metals of the first column 0! the 111th group of the periodic system of elements (vanadium, eolumbium, tantalum). The amounts in which these elements may be contained in the alloy are as iollows:
sears seas:assessment; Mom 8%, Vanadium 15%. Columblum Tantalum The lower limit of these additions ls generally not below 0.3% and the upper limit of the additions together not above 15%. The alloys so modified can be subjected tostill higher mechanical load at high temperatures, that is to say the mechanical properties at a given temperature are better than those of the alloys without .the apeciiied additions, or the temperature at "which the alloys can stand a predetermined mechanical load may be higher.
The above mentioned annealing at excessive temperatures before use for improving the properties as regards creep limit at temperatures above the recrystallisation temperature, or the above mentioned 1orging, rolling, drawing, or hammering at temperatures between the recrystallisation temperature and the temperature particularly up to 5% atwhich thealloysaretobeused,iorthepurpose oi increasing the creep resistance at temperatures below the recrystallisation temperature and the surface hardening by means oi cold working can also be applied to the alloys with the additions of titanium, tantalum, columbium. vanadium, zirconium and thorium with good results. The composition of the alloys with the said additions so tar as the main constituents are concerned. lies within the limits given above. Thus a particularly advantageous alloy can be obtained with about 15 to 27% cobalt, 14 to 17% chromium, 6 to 16% iron, 5 to 7% molybdenum, 0 to 7% tungsten, especially 3 to 7% tungsten, besides nickels also main constituents, with additions of up to 5% titanium, up to 15% tantalum, up to 15% columbium, up to 8% thorium, and possibly the usual deoxidising and manuiacturing additions.
We claim:
Method of hardening an alloy consisting of from 14 to 17% chromium, 14 to 16% iron, 5 to 7% molybdenum, 0.05 to 7% tungsten, 15 to 27% cobalt, and 52 to 27% nickel, which method consists in cold working the said alloy.
WILHELM ROHIN'. HEINRICH CORNELIUS. FRANZ BOLLENRATH;
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US362236A US2247643A (en) | 1938-12-24 | 1940-10-22 | Hardening cobalt-nickel-chromium-iron alloys |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US247696A US2245366A (en) | 1938-07-26 | 1938-12-24 | Hardening cobalt-nickel-chromiumiron alloys |
US362236A US2247643A (en) | 1938-12-24 | 1940-10-22 | Hardening cobalt-nickel-chromium-iron alloys |
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US2247643A true US2247643A (en) | 1941-07-01 |
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US362236A Expired - Lifetime US2247643A (en) | 1938-12-24 | 1940-10-22 | Hardening cobalt-nickel-chromium-iron alloys |
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2542266A (en) * | 1946-10-07 | 1951-02-20 | Int Nickel Co | Heat and creep resisting nickel alloy castings |
US2951757A (en) * | 1958-03-07 | 1960-09-06 | Westinghouse Electric Corp | High temperature nickel base alloy |
US2974036A (en) * | 1958-07-28 | 1961-03-07 | Sierra Metals Corp | High temperature cobalt-base alloy |
US2974037A (en) * | 1958-07-28 | 1961-03-07 | Sierra Metals Corp | High temperature cobalt base alloy |
US2977223A (en) * | 1957-12-10 | 1961-03-28 | Westinghouse Electric Corp | Stabilized and precipitation-hardened nickel-base alloys |
US3026199A (en) * | 1958-07-28 | 1962-03-20 | Sierra Metals Corp | Metal alloy |
US3085005A (en) * | 1958-01-16 | 1963-04-09 | Fansteel Metallurgical Corp | Alloys |
US3118763A (en) * | 1958-07-28 | 1964-01-21 | Sierra Metals Corp | Cobalt base alloys |
US3202506A (en) * | 1963-01-23 | 1965-08-24 | David E Deutsch | High-temperature oxidation-resistant cobalt base alloys |
US3220829A (en) * | 1961-10-10 | 1965-11-30 | Int Nickel Co | Cast alloy |
US3223818A (en) * | 1961-04-27 | 1965-12-14 | Smith Corp A O | Method of welding |
US3234015A (en) * | 1961-05-01 | 1966-02-08 | Dougles E Jones | Heavy duty, wear resistant machine element |
US3268327A (en) * | 1963-11-14 | 1966-08-23 | Union Carbide Corp | Alloys with high resistance to sea water corrosion |
US3361560A (en) * | 1966-04-19 | 1968-01-02 | Du Pont | Nickel silicon and refractory metal alloy |
US3493366A (en) * | 1965-11-12 | 1970-02-03 | Int Nickel Co | Alloy for service in petrochemical and hydrocarbon processing |
-
1940
- 1940-10-22 US US362236A patent/US2247643A/en not_active Expired - Lifetime
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2542266A (en) * | 1946-10-07 | 1951-02-20 | Int Nickel Co | Heat and creep resisting nickel alloy castings |
US2977223A (en) * | 1957-12-10 | 1961-03-28 | Westinghouse Electric Corp | Stabilized and precipitation-hardened nickel-base alloys |
US3085005A (en) * | 1958-01-16 | 1963-04-09 | Fansteel Metallurgical Corp | Alloys |
US2951757A (en) * | 1958-03-07 | 1960-09-06 | Westinghouse Electric Corp | High temperature nickel base alloy |
US2974036A (en) * | 1958-07-28 | 1961-03-07 | Sierra Metals Corp | High temperature cobalt-base alloy |
US2974037A (en) * | 1958-07-28 | 1961-03-07 | Sierra Metals Corp | High temperature cobalt base alloy |
US3026199A (en) * | 1958-07-28 | 1962-03-20 | Sierra Metals Corp | Metal alloy |
US3118763A (en) * | 1958-07-28 | 1964-01-21 | Sierra Metals Corp | Cobalt base alloys |
US3223818A (en) * | 1961-04-27 | 1965-12-14 | Smith Corp A O | Method of welding |
US3234015A (en) * | 1961-05-01 | 1966-02-08 | Dougles E Jones | Heavy duty, wear resistant machine element |
US3220829A (en) * | 1961-10-10 | 1965-11-30 | Int Nickel Co | Cast alloy |
US3202506A (en) * | 1963-01-23 | 1965-08-24 | David E Deutsch | High-temperature oxidation-resistant cobalt base alloys |
US3268327A (en) * | 1963-11-14 | 1966-08-23 | Union Carbide Corp | Alloys with high resistance to sea water corrosion |
US3493366A (en) * | 1965-11-12 | 1970-02-03 | Int Nickel Co | Alloy for service in petrochemical and hydrocarbon processing |
US3361560A (en) * | 1966-04-19 | 1968-01-02 | Du Pont | Nickel silicon and refractory metal alloy |
USRE29547E (en) * | 1966-04-19 | 1978-02-21 | E. I. Du Pont De Nemours And Company | Nickel silicon and refractory metal alloy |
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