US3318690A - Age hardening manganese-containing maraging steel - Google Patents
Age hardening manganese-containing maraging steel Download PDFInfo
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- US3318690A US3318690A US373871A US37387164A US3318690A US 3318690 A US3318690 A US 3318690A US 373871 A US373871 A US 373871A US 37387164 A US37387164 A US 37387164A US 3318690 A US3318690 A US 3318690A
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- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 title claims description 23
- 229910052748 manganese Inorganic materials 0.000 title claims description 23
- 239000011572 manganese Substances 0.000 title claims description 23
- 238000003483 aging Methods 0.000 title description 3
- 229910001240 Maraging steel Inorganic materials 0.000 title description 2
- 229910000831 Steel Inorganic materials 0.000 claims description 50
- 239000010959 steel Substances 0.000 claims description 50
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 32
- 229910000734 martensite Inorganic materials 0.000 claims description 19
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 229910052759 nickel Inorganic materials 0.000 claims description 16
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 11
- 229910052804 chromium Inorganic materials 0.000 claims description 11
- 239000011651 chromium Substances 0.000 claims description 11
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 10
- 229910052782 aluminium Inorganic materials 0.000 claims description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 10
- 239000010936 titanium Substances 0.000 claims description 10
- 229910052719 titanium Inorganic materials 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 9
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 8
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 5
- 229910052790 beryllium Inorganic materials 0.000 claims description 5
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- 239000011733 molybdenum Substances 0.000 claims description 5
- 239000010955 niobium Substances 0.000 claims description 5
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 5
- 229910052715 tantalum Inorganic materials 0.000 claims description 5
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 5
- 229910052720 vanadium Inorganic materials 0.000 claims description 5
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 229910017052 cobalt Inorganic materials 0.000 claims description 4
- 239000010941 cobalt Substances 0.000 claims description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 4
- 229910052721 tungsten Inorganic materials 0.000 claims description 4
- 239000010937 tungsten Substances 0.000 claims description 4
- 229910045601 alloy Inorganic materials 0.000 description 29
- 239000000956 alloy Substances 0.000 description 29
- 230000032683 aging Effects 0.000 description 12
- 229910001566 austenite Inorganic materials 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 238000000137 annealing Methods 0.000 description 6
- 230000009466 transformation Effects 0.000 description 6
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 238000005482 strain hardening Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
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- 238000010791 quenching Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 101100135641 Caenorhabditis elegans par-3 gene Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-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
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
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- 230000002349 favourable effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000009865 steel metallurgy Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
Definitions
- the present invention relates to ferrous-base alloys and, more particularly, to ferrous-base alloys manifesting a combination of relatively high yield strength and satisfactory toughness characteristics of sumcient magnitude that they are suitable for use, inter alia, as steels for high strength structural applications.
- Manganese is an element which is probably present in all carbon and low alloy steels. However, notwithstanding its extensive use in steels, manganese (insofar as we are aware) has not been proposed for the purpose of achieving relatively high yield strengths combined with a reasonable degree of toughness in age-hardenable, nonquenched steels. As is known, manganese is found as a residual element and often used as a refining agent in steels. For example, manganese is utilized to tie-up detrimental sulfur, whereby the subversive influence of sulfur is rendered innocuous.
- manganese promotes hardenability characteristics, particularly in quenched steels and also has been used in substantial amounts in the AISI 200 series of stainless steels. In the latter instance, it is used to stabilize austenite, a function which it also performs in the high manganese steels (circa 13% manganese), generally known as the Hadfield steels. Too, the use of manganese has also been advanced for producing expansion members of bi-metallic elements.
- the alloys of the present invention are of the class known as the maraging steels which were developed and introduced to the art several years ago. These steels have not only opened up a vast new area of steel metallurgy and technology but fundamentally differ from the carbon and low alloy steels in that upon heating (aging) in the martensitic condition, the maraging steels increase in hardness and strength as opposed to the softening response and decrease in strength attendant the carbon and low alloy steels.
- manganese while it has been deemed to be a hardener in such prior steels, amounts thereof on the order of, say, 0.5 and above have resulted in a rather marked impairment of ductility. This is not the case in accordance with the instant invention.
- the present invention contemplates providing alloy steels which are martensitic in the solution annealed condition and which thereafter can be age hardened in the martensitic condition to provide satisfactory levels of both yield strength and toughness.
- the alloy steels consist essentially of (by weight) about 10% to 20% nickel, about 1.2% to 3.9% manganese, up to 5% chromium, with the sum of the nickel plus manganese plus chromium contents being controlled such that the total sum thereof is from 14% to 23%, e.g., 16% to 22%, carbon in an amount up to 0.03%, up to 1% titanium, up to 1% aluminum with the sum of the titanium plus aluminum not exceeding 1%, up to 1% silicon, and the balance essentially iron.
- the steels most advantageously contain about 16% to about 20% nickel, about 1.5% to 3% manganese, up to 1% chromium, the sum of the nickel plus manganese plus chromium contents being about 17.5% to about 23%, carbon in an amount up to 0.03%, up to 0.5% titanium, e.g., 0.02% to 0.2% titanium, up to 0.5% aluminum, e.g., 0.02% to 0.2% aluminum, up to 0.5 silicon and the balance essentially iron.
- steels of the present invention exhibit yield strengths (0.2% offset) of from 150,000 to 225,000 pounds per square inch (p.s.i.) together with a highly satisfactory magnitude of toughness as determined by tensile elongation and reduction of area properties.
- the following auxiliary elements in a total aggregate of not more than 2% can be present: up to 2% cobalt, up to 2% molybdenum, up to 2% vanadium, up to 2% tungsten, up to 0.4% beryllium, up to 2% columbium, up to 2% tantalum and up to 2% copper.
- the nickel content is advantageously from 16% to 20%, e.g., 18%.
- Lower amounts of nickel result in lower strength levels whereas higher amounts promote retention of austenite upon cooling from solution annealing temperature to about room temperature, i.e., the structure obtained on cooling from solution (annealing) treatment may not be as completely ma-rtensitic as would otherwise be the case, thus necessitating, for example, a sub-zero cooling treatment to effect as complete a transformation to martensite as possible.
- the amount of manganese employed has been found to be most important. When the manganese content is less than about 1.2%, yield strength is adversely affected whereas with manganese contents above about 3.9%, toughness is detrimentally impaired.
- the manganese content advantageously should be within the range of 1.5% to 3%.
- the total content of nickel plus manganese should not exceed 23% since as referred to herein-above, retained austenite can ensue. Retained austenite, assuming that too much of this phase is not present, can be transformed by refrigerating or cold working at sub-zero temperatures before aging. It is preferred that at least small amounts, e.g., 0.02% to 0.2%, of titanium and/or aluminum be present in the steels to achieve optimum toughness characteristics.
- the amount of carbon advantageously should not exceed 0.03%. With carbon contents characteristics of various carbon and low alloy steels, toughness is impaired and higher strength levels are not attained.
- the steels should be substantially devoid of elements such as sulfur, phosphorus, oxygen, nitrogen, lead, etc., as is consistent with commercial steelmaking practice. Such constituents merely serve to give rise to problems involving processing of the steels, e.g., workability, and result in a deterioration of properties.
- a most advantageous range of composition for steels contemplated herein is as follows: 17.5% to 18.5% nick- 'el, e.g., 18% nickel, about 1.75% to 2.75% manganese,
- manganese e.g., 2.5%
- carbon in an amount up to 0.02%, e.g., 0.01%, and the balance essentially iron.
- a further attribute of the steels of the instant invention is that they can be prepared using standard air melting techniques. While vacuum melting treatments can be employed, air melting practice results in a satisfactory level of properties. Materials of relatively high purity and/or selected scrap should be used as the basic melting charge, and such metals as boron, zirconium, calcium, lithium, magnesium and the like can be used as suit-able m'alleableizing and/or deoxidizing constituents. Titanium also can be employed for this purpose. Cast ingots obtained upon solidification of the melt should be rather thoroughly homogenized by soaking at temperatures of r about 2200 F. to about 2400 F. followed by hot working and, if desired, by cold Working to size and/ or shape.
- the steels Prior to aging, the steels should be solution annealed at temperatures of from about 1400 F. to about 1600 F. High annealing temperatures up to 2300 F. can be employed but the higher annealing temperatures result in a loss of tensile strength although hardening is still possible with the utilization of such temperature levels.
- the alloys Upon cooling from the solution annealing treatment, the alloys transform from austenite to martensite. It is important that as complete a martensitic structure be obtained prior to aging in order to achieve the high strength levels characteristic of the steels.
- martensite or martensitic refers to steels having a structure of martensite (or substantially martensitic) in both the solution annealed condition and in the aged condition.
- the transformation from austenite to martensite is normally accomplished by cooling through the M -M transformation range to room temperature (from the annealing temperature). As indicated above, in some instances and in order to attain as complete a transformation as possible, it may be desirable to cool the steels below room temperature, e.g., down to min-us 100 'F., as by, for example, refrigeration. To illustrate, should the total content of nickel plus manganese plus any amount of chromium present exceed about 22%, sub-zero cooling would be beneficial. Cold Working prior to "aging can also be used to effect the completion of transformation to martensite.
- the aging treatment should be conducted over the temperature range of 700 F. to about 900 F. and preferably 750 F. to 850 F. for about 1 to 50 hours, e.g., 3 to 24 hours at 800 F. Aging temperatures appreciably above 900 F. should be avoided; otherwise, retention of undesired austenite can occur. Since aging temperatures of 700 F. require undesirably longer aging times, it is advantageous to use the aging temperature range of about 750 F. to 850 F.
- Bal. Ess.:balance of alloy was essentially iron.
- the steels were homogenized, hot forged and thereafter hot rolled to inch diameter bar stock. Specimens were solution annealed at 1500 F. for one hour and thereafter refrigerated for 16 hours at minus 105 F. to assure, as a precautionary measure, complete transformation to martensite. Thereafter the steels were aged at either 700 F., 800 F., or 900 F. for various periods and the data in Table II illustrate the hardness behavior thereof.
- the yield strength (Y.S., 0.2% offset) and ultimate tensile strength (U.T.S.) in thousands of pounds per square inch (K.S.I.), tensile elongation (EL, percent) and reduction of area (R.A., percent) characteristics are given in Table III for alloys A, 1 and 2.
- the steels were aged at 800 F. for a period of time as noted in Table III.
- the properties of alloy A are also given in the as-refrigerated condition.
- the present invention is particularly applicable to the 2.
- the alloy as set forth in claim 1 in which both titaproduction of high strength structural elements, assemblies nium and aluminum are present in an amount of 0.02% and the like.
- the aged alloys of the invention can be to 0.2%, respectively. used as sheet, plate, rods, bars, extrusion, etc.
- Amartsitic steel characterized in that it transforms ticular advantage of the contemplated alloys is that they substantially to martensite at room temperature or above can be readily machined and/or otherwise shaped or and further characterized in the aged condition by a comformed while in the annealed condition and can therebination of relatively high yield strength together with a after be age hardened Without the incurrence of detri- 2O satisfactory level of toughness, said steel consisting essenmental distortion or dimensional change being induced by tially of about 10% to nickel, from 1.2% to 3.9% the age-hardening treatment.
- cobalt, up to 2% molybdenum, up to 2% vanadium, up to the term balance as used herein in referring to the iron 2% tungsten, up to 0.4% beryllium, up to 2% columbium, content of the alloys does not preclude the presence of up to 2% tantalum, up to 2% copper, with the proviso that other elements, e.g., deoxidizing and cleansing elements, the total summation of cobalt, molybdenum, vanadium, and impurities normally associated therewith in small tungsten, beryllium, columbium, tantalum and copper is amounts which do not adversely afiect the basic characternot greater than 2%, and the balance essentially iron.
- a martensitic steel characterized in that it transforms UNITED STATES PATENTS substantially to martensite at room temperature or above 963,123 7/1910 F PP 75128 and further characterized in the aged condition by a com- 2,048,164 7/1936 Pllhng bination of relatively high yield strength together with a 2683677 7/1954 Walters 148-442 satisfactory level of toughness, said steel consisting essen- OTHER REFERENCES of about 16% to about 20% mckfeli aboflt 15% to The Journal of the Iron and Steel Institute, No.11, 1920, ⁇ b01111 3% manganese, P to 1% Chromium, Wlth the 511m volume CII, article by Hanson et al., pages 41 and 49-59.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Organic Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
Description
United States Patent 3,318,690 AGE HARDENIN G MANGANESE-CONTAINING MARAGING STEEL Stephen Floreen, Westfield, and Raymond Frank Decker, Fanwood, N.J., assignors to The International Nickel Company, Inc., New York, N.Y., a corporation of Delaware No Drawing. Filed June 9, 1964, Ser. No. 373,871 4 Claims. (Cl. 75-123) The present invention relates to ferrous-base alloys and, more particularly, to ferrous-base alloys manifesting a combination of relatively high yield strength and satisfactory toughness characteristics of sumcient magnitude that they are suitable for use, inter alia, as steels for high strength structural applications.
As is well known to those skilled in the art, a number of mild carbon and low alloy steels have been developed and/or proposed for use as structural steels in structural applications. Generally, such steels are normally of the quenched and tempered variety and are characterized by yield strengths on the order of about up to 100,000 pounds per square inch (p.s.i.) or above. There are any number of carbon-containing low alloy steels which afford yield strengths of 150,000 to 200,000 p.s.i. or above, but they generally lack adequate toughness and/or are afilicted with other problems to be utilized for diversified structural applications on a substantial commercial basis. For example, there are the well known problems of warpage and dimensional change attendant the quench operation, particularly with respect to fairly high carboncontaining steel-s. Too, weldability problems arise and embrittlement problems on cooling from tempering temperatures become a source of difiiculty.
A number of alloying constituents have been advanced to achieve high yield strengths together with adequate toughness in both the quenched and non-quenched steels. Manganese is an element which is probably present in all carbon and low alloy steels. However, notwithstanding its extensive use in steels, manganese (insofar as we are aware) has not been proposed for the purpose of achieving relatively high yield strengths combined with a reasonable degree of toughness in age-hardenable, nonquenched steels. As is known, manganese is found as a residual element and often used as a refining agent in steels. For example, manganese is utilized to tie-up detrimental sulfur, whereby the subversive influence of sulfur is rendered innocuous. Of course, manganese promotes hardenability characteristics, particularly in quenched steels and also has been used in substantial amounts in the AISI 200 series of stainless steels. In the latter instance, it is used to stabilize austenite, a function which it also performs in the high manganese steels (circa 13% manganese), generally known as the Hadfield steels. Too, the use of manganese has also been advanced for producing expansion members of bi-metallic elements.
However, it has now been discovered that when special amounts of manganese are incorporated in nickel-containing, ferrous base alloys, an age-hardenable steel is provided which affords, upon simple heat treatment, a satisfactory combination of yield strength and toughness. Further, alloys contemplated herein exhibit an unusually low hardness in the annealed condition. This renders the steels especially amenable to working and machining operations. This is in direct contrast to quenched steels wherein maximum hardness is obtained on quenching, a condition which is not favorable to ease of workability and machinability.
The alloys of the present invention are of the class known as the maraging steels which were developed and introduced to the art several years ago. These steels have not only opened up a vast new area of steel metallurgy and technology but fundamentally differ from the carbon and low alloy steels in that upon heating (aging) in the martensitic condition, the maraging steels increase in hardness and strength as opposed to the softening response and decrease in strength attendant the carbon and low alloy steels. In this connection it should be mentioned that with the advent of the maraging steels, manganese, while it has been deemed to be a hardener in such prior steels, amounts thereof on the order of, say, 0.5 and above have resulted in a rather marked impairment of ductility. This is not the case in accordance with the instant invention.
It is an object of the present invention to provide a novel manganese-containing, age-hardenable steel capable of providing relatively high yield strengths in combination with an acceptable level of toughness in the aged condition.
Other objects and advantages will become apparent from the following description.
Generally speaking, the present invention contemplates providing alloy steels which are martensitic in the solution annealed condition and which thereafter can be age hardened in the martensitic condition to provide satisfactory levels of both yield strength and toughness. The alloy steels consist essentially of (by weight) about 10% to 20% nickel, about 1.2% to 3.9% manganese, up to 5% chromium, with the sum of the nickel plus manganese plus chromium contents being controlled such that the total sum thereof is from 14% to 23%, e.g., 16% to 22%, carbon in an amount up to 0.03%, up to 1% titanium, up to 1% aluminum with the sum of the titanium plus aluminum not exceeding 1%, up to 1% silicon, and the balance essentially iron. To achieve an optimum combination of properties, including yield strength and toughness, the steels most advantageously contain about 16% to about 20% nickel, about 1.5% to 3% manganese, up to 1% chromium, the sum of the nickel plus manganese plus chromium contents being about 17.5% to about 23%, carbon in an amount up to 0.03%, up to 0.5% titanium, e.g., 0.02% to 0.2% titanium, up to 0.5% aluminum, e.g., 0.02% to 0.2% aluminum, up to 0.5 silicon and the balance essentially iron. When heat treated by aging, steels of the present invention exhibit yield strengths (0.2% offset) of from 150,000 to 225,000 pounds per square inch (p.s.i.) together with a highly satisfactory magnitude of toughness as determined by tensile elongation and reduction of area properties. The following auxiliary elements in a total aggregate of not more than 2% can be present: up to 2% cobalt, up to 2% molybdenum, up to 2% vanadium, up to 2% tungsten, up to 0.4% beryllium, up to 2% columbium, up to 2% tantalum and up to 2% copper.
In carrying the invention into practice, the nickel content is advantageously from 16% to 20%, e.g., 18%. Lower amounts of nickel result in lower strength levels whereas higher amounts promote retention of austenite upon cooling from solution annealing temperature to about room temperature, i.e., the structure obtained on cooling from solution (annealing) treatment may not be as completely ma-rtensitic as would otherwise be the case, thus necessitating, for example, a sub-zero cooling treatment to effect as complete a transformation to martensite as possible.
The amount of manganese employed has been found to be most important. When the manganese content is less than about 1.2%, yield strength is adversely affected whereas with manganese contents above about 3.9%, toughness is detrimentally impaired. For the best combination of properties, the manganese content advantageously should be within the range of 1.5% to 3%. However, the total content of nickel plus manganese should not exceed 23% since as referred to herein-above, retained austenite can ensue. Retained austenite, assuming that too much of this phase is not present, can be transformed by refrigerating or cold working at sub-zero temperatures before aging. It is preferred that at least small amounts, e.g., 0.02% to 0.2%, of titanium and/or aluminum be present in the steels to achieve optimum toughness characteristics.
The amount of carbon advantageously should not exceed 0.03%. With carbon contents characteristics of various carbon and low alloy steels, toughness is impaired and higher strength levels are not attained. The steels should be substantially devoid of elements such as sulfur, phosphorus, oxygen, nitrogen, lead, etc., as is consistent with commercial steelmaking practice. Such constituents merely serve to give rise to problems involving processing of the steels, e.g., workability, and result in a deterioration of properties.
A most advantageous range of composition for steels contemplated herein is as follows: 17.5% to 18.5% nick- 'el, e.g., 18% nickel, about 1.75% to 2.75% manganese,
e.g., 2.5% manganese, carbon in an amount up to 0.02%, e.g., 0.01%, and the balance essentially iron.
A further attribute of the steels of the instant invention is that they can be prepared using standard air melting techniques. While vacuum melting treatments can be employed, air melting practice results in a satisfactory level of properties. Materials of relatively high purity and/or selected scrap should be used as the basic melting charge, and such metals as boron, zirconium, calcium, lithium, magnesium and the like can be used as suit-able m'alleableizing and/or deoxidizing constituents. Titanium also can be employed for this purpose. Cast ingots obtained upon solidification of the melt should be rather thoroughly homogenized by soaking at temperatures of r about 2200 F. to about 2400 F. followed by hot working and, if desired, by cold Working to size and/ or shape.
Prior to aging, the steels should be solution annealed at temperatures of from about 1400 F. to about 1600 F. High annealing temperatures up to 2300 F. can be employed but the higher annealing temperatures result in a loss of tensile strength although hardening is still possible with the utilization of such temperature levels. Upon cooling from the solution annealing treatment, the alloys transform from austenite to martensite. It is important that as complete a martensitic structure be obtained prior to aging in order to achieve the high strength levels characteristic of the steels. As used herein, the term martensite (or martensitic) refers to steels having a structure of martensite (or substantially martensitic) in both the solution annealed condition and in the aged condition. The transformation from austenite to martensite is normally accomplished by cooling through the M -M transformation range to room temperature (from the annealing temperature). As indicated above, in some instances and in order to attain as complete a transformation as possible, it may be desirable to cool the steels below room temperature, e.g., down to min-us 100 'F., as by, for example, refrigeration. To illustrate, should the total content of nickel plus manganese plus any amount of chromium present exceed about 22%, sub-zero cooling would be beneficial. Cold Working prior to "aging can also be used to effect the completion of transformation to martensite.
The aging treatment should be conducted over the temperature range of 700 F. to about 900 F. and preferably 750 F. to 850 F. for about 1 to 50 hours, e.g., 3 to 24 hours at 800 F. Aging temperatures appreciably above 900 F. should be avoided; otherwise, retention of undesired austenite can occur. Since aging temperatures of 700 F. require undesirably longer aging times, it is advantageous to use the aging temperature range of about 750 F. to 850 F.
For the purpose of giving those skilled in the art a better understanding and/or a better "appreciation of the advantages of the invention, the following illustrative data are given:
A series of alloys having compositions given in Table I (Alloys A and B being outside the invention and Alloys 1 and 2 being within the invention) were prepared by air melting, small amounts of silicon, aluminum and titanium being used as refining additions.
Bal. Ess.:balance of alloy was essentially iron.
The steels were homogenized, hot forged and thereafter hot rolled to inch diameter bar stock. Specimens were solution annealed at 1500 F. for one hour and thereafter refrigerated for 16 hours at minus 105 F. to assure, as a precautionary measure, complete transformation to martensite. Thereafter the steels were aged at either 700 F., 800 F., or 900 F. for various periods and the data in Table II illustrate the hardness behavior thereof.
TABLE 11 Hardness, Rockwell C" Time (hours) The foregoing hardness data illustrate that prolonged heat particularly at a temperature of 900 F. results in overaging and possible formation of retained austenite, factors which should be, as noted above herein, avoided. Alloy B reflects that with manganese contents of 0.8%, an amount quite representative of many carbon and low alloy steels, the response to age hardening treatment is minimal. The hardness characteristics of this alloy were such that further testing with regard thereto was not conducted.
The yield strength (Y.S., 0.2% offset) and ultimate tensile strength (U.T.S.) in thousands of pounds per square inch (K.S.I.), tensile elongation (EL, percent) and reduction of area (R.A., percent) characteristics are given in Table III for alloys A, 1 and 2. In this regard, the steels were aged at 800 F. for a period of time as noted in Table III. The properties of alloy A are also given in the as-refrigerated condition.
TABLE III Alloy Aging Time, Heat 0.2% Otiset U.T.S. EL, R.A.,
No. hours Treatment,F Y.S. (k.s.i.) (k.s.i.) percent percent A 119 144 16 73 1 800 123 126 18 74 8 800 128 132 20 73 1 3 800 165 173 s as 2 3 800 212 21s 13 49 24 800 215 224 11 47 1 0.252 inch diameter, 1 inch gage length.
2 As refrigerated.
The present invention is particularly applicable to the 2. The alloy as set forth in claim 1 in which both titaproduction of high strength structural elements, assemblies nium and aluminum are present in an amount of 0.02% and the like. The aged alloys of the invention can be to 0.2%, respectively. used as sheet, plate, rods, bars, extrusion, etc. A par- 3. Amartensitic steel characterized in that it transforms ticular advantage of the contemplated alloys is that they substantially to martensite at room temperature or above can be readily machined and/or otherwise shaped or and further characterized in the aged condition by a comformed while in the annealed condition and can therebination of relatively high yield strength together with a after be age hardened Without the incurrence of detri- 2O satisfactory level of toughness, said steel consisting essenmental distortion or dimensional change being induced by tially of about 10% to nickel, from 1.2% to 3.9% the age-hardening treatment. The necessity of utilizing manganese, up to 5% chromium, the sum of the nickel further processing steps to obviate distortion and/or diplus manganese plus chromium contents being about 14% mensional change has been characteristic of prior art carto 23%, carbon in an amount up to 0.03%, up to 1% bon and low alloy steels. 25 titanium, up to 1% aluminum, up to 1% silicon, up to 2% As will be readily understood by those skilled in the art, cobalt, up to 2% molybdenum, up to 2% vanadium, up to the term balance as used herein in referring to the iron 2% tungsten, up to 0.4% beryllium, up to 2% columbium, content of the alloys does not preclude the presence of up to 2% tantalum, up to 2% copper, with the proviso that other elements, e.g., deoxidizing and cleansing elements, the total summation of cobalt, molybdenum, vanadium, and impurities normally associated therewith in small tungsten, beryllium, columbium, tantalum and copper is amounts which do not adversely afiect the basic characternot greater than 2%, and the balance essentially iron. istics of the alloys. 4. A martensitic steel characterized in that it transforms Although the present invention has been described in substantially to maftqnsite. at room p f f e or bove conjunction with preferred embodiments, it is to be underf fPrther charectenlqd 1n F aged condltlon y 9 stood that modifications and variations may be resorted 192 of i 2 hlghh yleld i l i l eag Wlth a to without departing from the spirit and scope of the in- 15 ac my CV o Dug Sal S Cons mg essen vention, as those skilled in the art will readily understand. ;9 g f to about 185% mckel about 175% Such modifications and variations are considered to be a on t up to 002% carbon and the alance essentially 11'01'1. w1th1n the purview and scope of the 1nvent1on and ap- 40 perxivded lclalms. References Cited by the Examiner e c aun:
1. A martensitic steel characterized in that it transforms UNITED STATES PATENTS substantially to martensite at room temperature or above 963,123 7/1910 F PP 75128 and further characterized in the aged condition by a com- 2,048,164 7/1936 Pllhng bination of relatively high yield strength together with a 2683677 7/1954 Walters 148-442 satisfactory level of toughness, said steel consisting essen- OTHER REFERENCES of about 16% to about 20% mckfeli aboflt 15% to The Journal of the Iron and Steel Institute, No.11, 1920, {b01111 3% manganese, P to 1% Chromium, Wlth the 511m volume CII, article by Hanson et al., pages 41 and 49-59.
of the nickel plus manganese plus chromium contents being about 17.5% to about 23%, up to 0.03% carbon, up to 0.5% titanium, up to 0.5 aluminum, up to 0.5 silicon, and the balance essentially iron.
HYLAND BIZOT, Primary Examiner. P. WEINSTEIN, Assistant Examiner.
Claims (1)
- 3. A MARTENSITIC STEEL CHARACTERIZED IN THAT IT TRANSFORMS SUBSTANTIALLY TO MARTENSITE AT ROOM TEMPERATURE OR ABOVE AND FURTHER CHARACTERIZED IN THE AGED CONDITION BY A COMBINATION OF RELATIVELY HIGH YIELD STRENGTH TOGETHER WITH A SATISFACTORY LEVEL OF THOUGHNESS, AND STELL CONSISTING ESSENTIALLY OF ABOUT 10% TO 20% NICKEL, FROM 1.2% TO 3.9% MANGANESE, UP TO 5% CHROMIUM, THE SUM OF THE NICKEL PLUS MANGANESE PLUS CHROMIUM CONTENTS BEING ABOUT 14% TO 23%, CARBON IN AN AMOUNT UP TO 0.03%, UP TO 1% TITANIUM, UP TO 1% ALUMINUM, UP TO 1% SILICON, UP TO 2% COBALT, UP TO 2% MOLYBDENUM, UP TO 2% VANADIUM, UP TO 2% TUNGESTEN, UP TO 0.4% BERYLLIUM, UP TO 2% COLUMBIUM, UP TO 2% TANTALUM, UP TO 2% COPPER, WITH THE PROVISO THAT THE TOTAT SUMMATION OF COBLAT, MOLYBDENUM, VANADIUM, TUNGSTEN, BERYLLIUM, COLUMBIUM, TANTALUM AND COPPER IS NOT GREATER THAN 2%, AND THE BALANCE ESSENTIALLY IRON.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US373871A US3318690A (en) | 1964-06-09 | 1964-06-09 | Age hardening manganese-containing maraging steel |
| GB22802/65A GB1046054A (en) | 1964-06-09 | 1965-05-28 | Alloy steel |
| DEJ28296A DE1221022B (en) | 1964-06-09 | 1965-06-05 | Martensite-hardenable steel alloy |
| FR19905A FR1443486A (en) | 1964-06-09 | 1965-06-08 | Alloy steel |
| BE665144D BE665144A (en) | 1964-06-09 | 1965-06-09 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US373871A US3318690A (en) | 1964-06-09 | 1964-06-09 | Age hardening manganese-containing maraging steel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3318690A true US3318690A (en) | 1967-05-09 |
Family
ID=23474234
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US373871A Expired - Lifetime US3318690A (en) | 1964-06-09 | 1964-06-09 | Age hardening manganese-containing maraging steel |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3318690A (en) |
| BE (1) | BE665144A (en) |
| DE (1) | DE1221022B (en) |
| FR (1) | FR1443486A (en) |
| GB (1) | GB1046054A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3365342A (en) * | 1965-06-15 | 1968-01-23 | Foote Mineral Co | Alloy steel and its preparation |
| US3392012A (en) * | 1965-06-04 | 1968-07-09 | Foote Mineral Co | Alloy steel and its preparation |
| US3770394A (en) * | 1970-09-14 | 1973-11-06 | Crucible Inc | Stainless steel tubing with a maximum titanium to carbon ratio of 6 |
| US4013425A (en) * | 1975-06-26 | 1977-03-22 | Metallgesellschaft Aktiengesellschaft | Thermometric bimetallic structure of high strength at high temperature |
| US4443254A (en) * | 1980-10-31 | 1984-04-17 | Inco Research & Development Center, Inc. | Cobalt free maraging steel |
| US4832909A (en) * | 1986-12-22 | 1989-05-23 | Carpenter Technology Corporation | Low cobalt-containing maraging steel with improved toughness |
| US4871511A (en) * | 1988-02-01 | 1989-10-03 | Inco Alloys International, Inc. | Maraging steel |
| US20040060622A1 (en) * | 2002-10-01 | 2004-04-01 | Lilley John David | Graphite and nitrogen-free cast alloys |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0023398B1 (en) * | 1979-07-10 | 1985-03-20 | National Research Development Corporation | Manganese steels and a process of making these steels |
| DE102007047016A1 (en) * | 2007-10-01 | 2009-04-02 | Robert Bosch Gmbh | Inexpensive, high-strength, martensitically hardenable steel, useful for producing automobile fuel injector components, has low alloying element content and is free of cobalt |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US963123A (en) * | 1910-02-01 | 1910-07-05 | Gen Electric | Electrical-resistance alloy. |
| US2048164A (en) * | 1931-08-31 | 1936-07-21 | Int Nickel Co | Method of treating alloys |
| US2683677A (en) * | 1942-07-27 | 1954-07-13 | Jr Francis M Walters | Method of precipitation hardening iron alloys |
-
1964
- 1964-06-09 US US373871A patent/US3318690A/en not_active Expired - Lifetime
-
1965
- 1965-05-28 GB GB22802/65A patent/GB1046054A/en not_active Expired
- 1965-06-05 DE DEJ28296A patent/DE1221022B/en active Pending
- 1965-06-08 FR FR19905A patent/FR1443486A/en not_active Expired
- 1965-06-09 BE BE665144D patent/BE665144A/xx unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US963123A (en) * | 1910-02-01 | 1910-07-05 | Gen Electric | Electrical-resistance alloy. |
| US2048164A (en) * | 1931-08-31 | 1936-07-21 | Int Nickel Co | Method of treating alloys |
| US2683677A (en) * | 1942-07-27 | 1954-07-13 | Jr Francis M Walters | Method of precipitation hardening iron alloys |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3392012A (en) * | 1965-06-04 | 1968-07-09 | Foote Mineral Co | Alloy steel and its preparation |
| US3365342A (en) * | 1965-06-15 | 1968-01-23 | Foote Mineral Co | Alloy steel and its preparation |
| US3770394A (en) * | 1970-09-14 | 1973-11-06 | Crucible Inc | Stainless steel tubing with a maximum titanium to carbon ratio of 6 |
| US4013425A (en) * | 1975-06-26 | 1977-03-22 | Metallgesellschaft Aktiengesellschaft | Thermometric bimetallic structure of high strength at high temperature |
| US4443254A (en) * | 1980-10-31 | 1984-04-17 | Inco Research & Development Center, Inc. | Cobalt free maraging steel |
| US4832909A (en) * | 1986-12-22 | 1989-05-23 | Carpenter Technology Corporation | Low cobalt-containing maraging steel with improved toughness |
| US4871511A (en) * | 1988-02-01 | 1989-10-03 | Inco Alloys International, Inc. | Maraging steel |
| US20040060622A1 (en) * | 2002-10-01 | 2004-04-01 | Lilley John David | Graphite and nitrogen-free cast alloys |
| WO2004031419A1 (en) * | 2002-10-01 | 2004-04-15 | Magotteaux International S.A. | Graphite and nitrogen-free cast alloys |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1443486A (en) | 1966-06-24 |
| BE665144A (en) | 1965-12-09 |
| DE1221022B (en) | 1966-07-14 |
| GB1046054A (en) | 1966-10-19 |
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