AU2013355066B2

AU2013355066B2 - High strength precipitation hardenable stainless steel

Info

Publication number: AU2013355066B2
Application number: AU2013355066A
Authority: AU
Inventors: Michael L. Schmidt; David E. Wert
Original assignee: CRS Holdings LLC
Current assignee: CRS Holdings LLC
Priority date: 2012-12-06
Filing date: 2013-12-06
Publication date: 2016-11-03
Anticipated expiration: 2033-12-06
Also published as: KR20150082614A; CA2893272A1; US20160319406A1; JP2016504498A; JP6117372B2; US20140161658A1; AU2013355066A1; KR101780875B1; EP2929062A1; CA2893272C; CN105102649A; US20180320256A1; BR112015013006A2; WO2014089418A1

Abstract

A precipitation hardenable, martensitic stainless steel alloy is disclosed. The alloy has the following composition in weight percent, about C 0.03 max Mn 1.0 max Si 0.75 max P 0.040 max s 0.020 max Cr 10 - 13 Ni 10.5 - 11.6 Mo 0.25 - 1.5 Co 0.5-1.5 Cu 0.75 max Ti 1.5 - 1.8 Al 0.3 - 0.8 Nb 0.3 - 0.8 B 0.010 max N 0.030 max The balance is iron and usual impurities. The disclosed alloy provides a unique combination of corrosion resistance, strength, and toughness.

Description

2013355066 14 Oct 2016

TITLE OF THE INVENTION

HIGH STRENGTH PRECIPITATION HARDENABLE STAINLESS STEEL BACKGROUND OF THE INVENTION: 5 Field of the Invention

This invention relates to precipitation hardenable, martensitic stainless steel alloys and in particular to a martensitic stainless steel alloy. Also described is an article made therefrom, having a novel combination of strength and corrosion resistance.

Description of the Related Art 10 The aerospace industry has been looking for a stainless steel alloy for landing gear for many years. The main alloy currently used for the commercial landing gear application is 300M alloy. 300M alloy can be quenched and tempered to provide an ultimate tensile strength of at least 280 ksi and fracture toughness (Kic) of at least 50 ksiVin. However, 300M alloy does not provide effective corrosion resistance. Therefore, it has been necessary to 15 plate the landing gear components with a corrosion resistant metal such as cadmium. Cadmium is a highly toxic, carcinogenic material and its use has presented significant environmental risks in the manufacture and maintenance of aircraft landing gear and other components made from 300M alloy. 20 Precipitation hardenable stainless steel alloys having commercially acceptable combinations of strength and toughness are known and used for various aerospace applications. However, some of those alloys do not provide strength equivalent to 300M, so they cannot be considered as “drop-in” replacements for that alloy. The other known precipitation hardenable stainless steels may provide adequate strength for the landing gear 25 application, but leave something to be desired in the resistance to corrosion they provide.

The corrosion resistance desired for the aircraft landing gear application includes general corrosion resistance, pitting corrosion resistance, and resistance to stress corrosion cracking.

In view of the foregoing discussion, there is a need for a steel alloy with mechanical 30 properties comparable to those of 300M, so the new alloy can be used as a drop-in -1- 2013355066 14 Oct 2016 replacement, combined with effective corrosion resistance in the variety of environments in which commercial aircraft are used.

SUMMARY OF THE INVENTION 5 The disadvantages associated with the known precipitation hardenable, martensitic stainless steel alloys are solved to a large degree by the alloy in accordance with the present invention; and/or the present invention at least provides the public with a useful choice. The alloy according to the present invention is a precipitation hardening Cr-Ni-Ti-Mo martensitic stainless steel alloy that provides a unique combination of strength, toughness, and corrosion 10 resistance.

In one aspect, the invention provides a precipitation hardenable, martensitic stainless steel alloy comprising in weight percent, about C 0.03 max 15 Mn 1.0 max Si 0.75 max P 0.040 max s 0.0.005 max Cr 10- 13 20 Ni 10.75 - 11.6 Mo 0.25 - 1.5 Cu 0.25 max Co 0.9-1.5 Ti 1.5 - 1.8 25 A1 0.4-0.8 Cb 0.3-0.8 B 0.010 max N 0.030 max and the balance is iron and usual impurities. 30 In another aspect, the invention provides a precipitation hardenable, martensitic stainless steel alloy comprising in weight percent, about C 0.02 max Mn 0.25 max Si 0.25 max 35 P 0.015 max -2- s 0.005 max Cr 10.5 - 12.5 Ni 10.75 - 11.25 Mo 0.75 - 1.25 Cu 0.25 max Co 0.9-1.25 Ti 1.5 - 1.7 A1 0 1 o Cb 0.4 - 0.7 B 0.001 - 0.005 N 0.015 max 2013355066 14 Oct 2016 and the balance is iron and usual impurities.

In another aspect, the invention provides precipitation hardenable, martensitic stainless steel alloy consisting essentially of, in weight percent, about 15 C 0.015 max Mn 0.10 max Si 0.10 max P 0.010 max s 0.005 max 20 Cr 11.0- 12.0 Ni 10.85 - 11.25 Mo 0.9-1.1 Co 0 1 Cu 0.25 max 25 Ti 1.5 - 1.7 A1 0.45 - 0.65 Cb 0.4-0.6 B 0.0015 - 0.0035 N 0.010 max 30 and the balance is iron and usual impurities.

Certain statements that appear below are broader than what appears in the statements of the invention above. These statements are provided in the interests of providing the reader with a better understanding of the invention and its practice. The reader is directed to the accompanying claim set which defines the scope of the invention. 35 -3- 2013355066 14 Oct 2016 c Broad 0.03 max Mn 1.0 max Si 0.75 max P 0.040 max s 0.020 max Cr 10-13 Ni 10.5-11.6 Mo 0.25 - 1.5 Cu 0.75 max Co 0.5-1.5 Ti 1.5-1.8 A1 0.3-0.8 Cb 0.3-0.8 B 0.010 max N 0.030 max

The broad, intermediate, and preferred compositional ranges of the alloy according to the present invention are set forth below in weight percent.

Intermediate 0.02 max 0.25 max 0.25 max 0.015 max 0.010 max 10.5 - 12.5 10.75 - 11.25 0.75 - 1.25 0.50 max 0.75-1.25 1.5 - 1.7 0.4-0.7 0.4-0.7 0.001 - 0.005 0.015 max

Preferred 0.015 max 0.10 max 0.10 max 0.010 max 0.005 max 11.0- 12.0 10.85 - 11.25 0.9-1.1 0.25 max 0.9-1.1 1.5 - 1.7 0.45-0.65 0.4-0.6 0.0015 - 0.0035 0.010 max

The balance of the alloy is essentially iron except for the usual impurities found in 5 commercial grades of such steels and minor amounts of additional elements which may vary from a few thousandths of a percent up to larger amounts that do not adversely affect the desired combination of properties provided by this alloy.

The foregoing tabulation is provided as a convenient summary and is not intended thereby to restrict the lower and upper values of the ranges of the individual elements of the 10 alloy of this invention for use in combination with each other, or to restrict the ranges of the elements for use solely in combination with each other. Thus, one or more of the element ranges of the broad composition can be used with one or more of the other ranges for the remaining elements in the preferred composition. In addition, a minimum or maximum for an element of one preferred embodiment can be used with the maximum or minimum for that 15 element from another preferred embodiment. Moreover, the alloy according to this invention may comprise, consist essentially of, or consist of the constituent elements described above and throughout this specification. Here and throughout this application, unless otherwise indicated, the term percent or the symbol means percent by weight or mass percent. -4- 2013355066 14 Oct 2016 DETAILED DESCRIPTION:

The alloy according to the present invention provides a unique combination of strength, toughness, and corrosion resistance which results from a novel balancing of the 5 elements chromium, nickel, cobalt, molybdenum and also the elements titanium, aluminum, and columbium. At least about 10%, better yet at least about 10.5%, and preferably at least about 11.0% chromium is present in the alloy to provide corrosion resistance similar to that of a conventional stainless steel. At least about 10.5%, better yet at least about 10.75%, and preferably at least about 10.85% nickel is present in the alloy because nickel benefits the 10 toughness and notch toughness of the alloy. Nickel also contributes to the corrosion resistance by enhancing the ability of the alloy to repassivate. This alloy contains at least about 0.5%, better yet at least about 0.75%, and preferably at least about 0.9% cobalt because cobalt contributes to the high strength and corrosion resistance provided by the alloy. At least about 0.25%, better yet at least about 0.75%, and preferably at least about 0.9% 15 molybdenum is also present in the alloy because molybdenum contributes to the alloy's notch toughness. Molybdenum also benefits the alloy's corrosion resistance in reducing media and in environments which promote pitting attack and stress-corrosion cracking.

The alloy of this invention also contains at least about 1.5% titanium to benefit the 20 strength of the alloy through the precipitation of a nickel-titanium-rich phase during aging. Columbium and aluminum also contribute to the strength provided by this alloy. Therefore, the alloy contains at least about 0.3% and better yet at least about 0.4% of each of columbium and aluminum. Preferably the alloy contains at least about 0.45% aluminum. 25 When chromium, nickel, cobalt, molybdenum, titanium, columbium, and aluminum are not properly balanced, the alloy's ability to transform fully to a martensitic structure using conventional processing techniques is inhibited. Furthermore, the alloy's ability to remain substantially fully martensitic when solution treated and age-hardened is impaired. Under such conditions the strength provided by the alloy is significantly reduced. Therefore, the 30 amounts of chromium, nickel, cobalt, molybdenum, titanium, columbium, and aluminum present in this alloy are restricted. More particularly, chromium is limited to not more than -5- 2013355066 14 Oct 2016 about 13%, better yet to not more than about 12.5%, and preferably to not more than about 12.0%. Nickel is limited to not more than about 11.6% and preferably to not more than about 11.25%. Too much cobalt adversely affects the strength and toughness provided by this alloy. Therefore, cobalt is restricted to not more than about 1.5%, better yet to not more than 5 about 1.25%, and preferably to not more than about 1.1%. Molybdenum is restricted to not more than about 1.5%, better yet to not more than about 1.25%, and preferably to not more than about 1.1%.

Too much titanium adversely affects the toughness and notch toughness of the alloy. 10 Therefore, titanium is restricted to not more than about 1.8% and preferably to not more than about 1.7% in this alloy. Too much aluminum can adversely affect the toughness and corrosion resistance provided by the alloy. Therefore, aluminum is restricted to not more than about 0.8%, better yet to not more than about 0.7%, and preferably to not more than about 0.65%. Too much columbium is likely to result in undesirable alloy segregation and 15 the precipitation of unwanted secondary phases such as Laves phase. Therefore, columbium is restricted to not more than about 0.8%, better yet to not more than about 0.7%, and preferably to not more than about 0.6% in this alloy.

Additional elements such as manganese, silicon, and boron may be present in 20 controlled amounts to benefit other desirable properties provided by this alloy. More specifically, up to about 1.0%, better yet up to about 0.5%, still better up to about 0.25%, and preferably up to about 0.10% manganese and/or up to about 0.75%, better yet up to about 0.5%, still better up to about 0.25%, and preferably up to about 0.10% silicon can be present in the alloy as residuals from scrap sources or deoxidizing additions. Such additions are 25 beneficial when the alloy is not vacuum melted. Manganese and/or silicon are preferably kept at low levels because of their adverse effect on toughness, corrosion resistance, and the austenite-martensite phase balance in the matrix material.

Up to about 0.010% boron, better yet up to about 0.005% boron, and preferably up to about 0.0035% boron can be present in the alloy to benefit the hot workability of the alloy. 30 In order to provide the desired effect, at least about 0.001% and preferably at least about 0.0015% boron is present in the alloy. -6- 2013355066 14 Oct 2016

The balance of the alloy is essentially iron apart from the usual impurities inevitably found in commercial grades of alloys intended for similar service or use. The levels of such elements are controlled so as not to adversely affect the desired properties.

In particular, too much carbon and/or nitrogen impair the corrosion resistance and 5 adversely affect the toughness provided by this alloy. Accordingly, not more than about 0.03%, better yet not more than about 0.02%, and preferably not more than about 0.015% carbon is present in the alloy. Also, not more than about 0.030%, better yet not more than about 0.015%, not more than about 0.010% nitrogen is present in the alloy. When carbon and/or nitrogen are present in larger amounts, the carbon and/or nitrogen bond with titanium, 10 aluminum, and/or columbium to form undesirable non-metallic inclusions such as carbides or nitrides and/or carbonitrides. Those reactions inhibit the formation of the nickel-titanium/aluminum/columbium intermetallic phases which are a primary factor in the development of the high strength provided by this alloy. 15 Phosphorus is maintained at a low level because of its adverse effect on toughness and corrosion resistance. Accordingly, not more than about 0.040%, better yet not more than about 0.015%, and preferably not more than about 0.010% phosphorus is present in the alloy.

Not more than about 0.020%, better yet not more than about 0.010%, and preferably 20 not more than about 0.005% sulfur is present in the alloy. Larger amounts of sulfur promote the formation of non-metallic sulfide inclusions which, like carbon and nitrogen, inhibit the desired strengthening effect provided by titanium, aluminum, and columbium. These sulfide inclusions impair the toughness of the alloy, especially in the transverse direction. Also, a greater amount of sulfur adversely affects the hot workability and corrosion resistance of this 25 alloy.

Although sulfur and phosphorus can be reduced to very low levels through the selection of high purity charge materials or by employing alloy refining techniques, their presence in the alloy cannot be entirely avoided under large scale production conditions. 30 Therefore, a small amount of calcium may be added in controlled amounts to combine with phosphorus and/or sulfur to facilitate the removal and stabilization of those two elements in -7- 2013355066 14 Oct 2016 the alloy. Calcium is also used to deoxidize the alloy. When used, the retained amount of calcium is not more than about 0.010% and preferably to not more than about 0.005% in this alloy. As an alternative to the calcium treatment, one or more rare earth metals (REM), particularly cerium and lanthanum, can be added to the alloy. In this regard, the alloy may 5 contain at least about 0.001% REM and better yet, at least about 0.002% REM. Too much REM recovery adversely affects the hot workability and the toughness of this alloy.

Excessive REM content also results in the formation of undesirable oxide inclusions in the alloy. Therefore, the amount of REM present in this alloy is limited to not more than about 0.025%, better yet to not more than about 0.015%, and preferably to not more than about 10 0.010%, in this alloy. It is further contemplated that magnesium can be added as an alternative to calcium or REM for desulfurization and deoxidation.

Too much copper adversely affects the notch toughness, ductility, and strength of this alloy. Therefore, the alloy contains not more than about 0.75%, better yet not more than 15 about 0.50%, and preferably not more than about 0.25% copper.

No special techniques are required for melting, casting, or working the alloy of the present invention. Vacuum induction melting (VIM) and vacuum induction melting followed by vacuum arc remelting (VAR) are the preferred methods of melting and refining this alloy, 20 but other practices can be used. In addition, this alloy can be made using powder metallurgy techniques, if desired. Further, although the alloy of the present invention can be hot or cold worked, cold working enhances the mechanical strength of the alloy.

The preferred method of providing calcium in this alloy is through the addition of a 25 nickel-calcium compound during VIM. The nickel-calcium compound, such as the Ni-Cal® alloy sold by Chemalloy Co. Inc., is added in an amount effective to combine with available phosphorus, sulfur, and oxygen. Other techniques for adding calcium may also be used. For example, capsules of elemental calcium or calcium master alloys can be added to the melt. It is believed that a slag containing calcium or a calcium compound may also be used. The 30 chemical reactions result in the formation of secondary phase inclusions such as calcium sulfides, calcium oxides, and calcium oxysulfides that are readily removed during primary or -8- 2013355066 14 Oct 2016 secondary melting. When used, REM are added to the molten alloy in the form of mischmetal which is a mixture of rare earth elements, an example of which contains about 50% cerium, about 30% lanthanum, about 15% neodymium, and about 5% praseodymium. 5 The precipitation hardenable alloy of the present invention is processed in multiple steps to develop the desired combination of properties. In a first step, the alloy is solution annealed. The solution annealing temperature is selected to be high enough to dissolve essentially all of the undesired precipitates into the alloy matrix material and to ensure that the grain structure is fully recrystallized. Unrecrystallized grains can lead to increased 10 anisotropy of the mechanical properties, particularly the ductility and toughness, of the alloy. However, if the solution annealing temperature is too high, it will impair the fracture toughness of the alloy by promoting excessive grain growth. Preferably, the alloy of the present invention is solution annealed at 1850°F - 1950°F (1010°C - 1066°C) for a time sufficient to substantially completely dissolve any precipitates in the alloy matrix and to fully 15 recrystallize the grain structure. The time at the solution temperature depends on the thickness of the part. The alloy is then quenched, preferably in oil.

To further develop the high strength of the alloy, it is subjected to a refrigeration treatment after it is quenched. The refrigeration treatment cools the alloy to a temperature 20 sufficiently below the martensite finish temperature to ensure the completion of the martensite transformation. Preferably, the refrigeration treatment comprises cooling the alloy to about -100°F (-73°C) or lower for a time sufficient to ensure that the alloy has substantially completely transformed to martensite. The need for a refrigeration treatment will be affected, at least in part, by the martensite finish temperature of the alloy. If the martensite 25 finish temperature is sufficiently high, the transformation to a martensitic structure can proceed without the need for a refrigeration treatment. In addition, the need for a refrigeration treatment may also depend on the section size of the piece being manufactured. As the section size of the piece increases, segregation in the alloy becomes more significant and the use of a refrigeration treatment becomes more beneficial. Further, the length of time 30 that the piece is chilled may need to be increased for large pieces in order to complete the transformation to martensite. For example, it has been found that a refrigeration treatment -9- 2013355066 14 Oct 2016 lasting a minimum of about 8 hours is preferred for developing the high strength that is characteristic of this alloy.

The alloy of the present invention is age hardened in accordance with techniques used 5 for the known precipitation hardening, stainless steel alloys, which treatments are known to those skilled in the art. For example, the alloys are preferably aged at about 950-975°F (510-524°C) for a time sufficient to ensure that the alloy is substantially uniformly heated to the aging temperature depending on the thickness of the part and typically for an additional 4 to 8 hours to complete the aging reaction and to reach the desired combination of strength and 10 toughness. The specific aging temperature used is selected by considering that: (1) the ultimate tensile strength of the alloy decreases as the aging temperature increases; and (2) the time required to age harden the alloy to a desired strength level increases as the aging temperature decreases. 15 The alloy of the present invention can be formed into a variety of product shapes for a wide variety of uses and lends itself to the formation of billets, bars, rod, wire, strip, plate, or sheet using conventional practices. The alloy of the present invention is useful in a wide range of practical applications which require an alloy having a good combination of corrosion resistance, strength, and toughness. In particular, the alloy of the present invention 20 can be used to produce structural members for aircraft, including but not limited to landing gear components and fasteners. The alloy is also well suited for use in medical and dental applications such as dental tools and medical scrapers, cutters, and suture needles.

Working Examples

In order to demonstrate the novel combination of strength, toughness, and corrosion 25 resistance provided by the alloy according to this invention, a comparative testing program was carried out. Seven 35 lb. heats having the weight percent compositions set forth in Table I below were produced by VIM.

TABLE I

Elmt. Ex. 1 Ex. 2 Ex. A Ex. B. Ex. C Ex. D. Ex. E -10- 2013355066 14 Oct 2016 c 0.002 0.003 0.005 0.002 0.002 0.002 0.003 Mn <0.01 <0.01 <0.01 <0.01 <0.01 <0.01 <0.01 Si <0.01 <0.01 0.04 <0.01 <0.01 <0.01 <0.01 P <0.005 <0.005 0.005 <0.005 <0.005 <0.005 <0.005 s 0.0006 0.0005 0.0009 0.0005 0.0005 0.0005 0.0005 Cr 11.42 11.49 11.35 11.48 11.47 11.47 11.47 Ni 11.04 10.66 10.86 11.01 11.04 10.41 10.00 Mo 0.95 0.95 0.94 0.95 0.95 0.95 0.95 Co 0.98 0.98 (Note) 1.96 2.94 1.96 2.94 Ti 1.63 1.62 1.54 1.63 1.65 1.63 1.63 A1 0.55 0.57 0.07 0.53 0.50 0.54 0.54 Cb 0.50 0.51 <0.01 0.51 0.54 0.50 0.51 B 0.0021 0.0019 0.0023 0.0019 0.0021 0.0021 0.0022 N 0.0015 0.0014 0.0013 0.0011 0.0014 0.0015 0.0015 Ca 0.0019 0.0021 0.0006 0.0021 0.0019 0.0019 0.0021 Note: No positive addition.

The balance of each heat is iron and usual impurities. Example 1 is representative of the alloy according to the present invention. Examples 2 and A to E are comparative alloys. In 5 particular, Example A is within the scope of the alloy described in US Patent No. 5,681,528.

The VIM heats were melted and cast into 4” square ingots. The ingots were charged into a furnace operating at 1500°F and the furnace temperature was ramped up to 2300°F. Ingots were held at 2300°F for 16 hours after which the furnace temperature was lowered to 10 2000°F. The ingots were held at 2000°F until they were substantially fully equalized in temperature. The ingots were then double-end forged to 2-3/4” square billet from starting temperature of 2000°F and then hot cut into 3 pieces each. Pieces were re-heated at 2000°F, and double-end forged to 1-1/4” square. The bars were again hot cut into 3 pieces and reheated at 2000°F. The bars were then single-end forged to 11/16” square with no reheats. 15 The bars were cooled in air, overage annealed at 1250°F for 8 hours, and then air cooled. -11- 2013355066 14 Oct 2016

Longitudinal smooth and notched (Kt =3) tensile samples, longitudinal Charpy V-notch (CVN) samples, and longitudinal rising step load (RSL) fracture toughness samples were machined from the bars of each heat. The samples from Examples 1, 2, B, C, D, and E were solution treated at 1900°F for 1 hour and oil quenched. The samples from Example A 5 were solution treated at 1800°F in accordance with the usual practice for that alloy. After solution treatment, all samples were refrigerated at -100°F for 24 hours then warmed in air to room temperature. The samples were then age-hardened at various temperatures ranging from 900°F to 1000°F. Aging was conducted by holding the samples at temperature for 4 hours in air and then quenching the samples in water. 10

The results of room temperature tensile testing on the samples of each heat are shown in Tables IIA and IIB below including the 0.2% offset yield strength (Y.S.) and the ultimate tensile strength (U.T.S) in ksi, the percent elongation (%E1.), the percent reduction in area (%R.A.), and the notch tensile strength (N.T.S.) in ksi.

15 TABLE IIA

Heat Solution Age Y.S. U.T.S. %EI. %R.A. N.T.S. — — — — 900°F 257 280 7.1 29.5 257 283 6.6 28.8 255 280 9.1 36.6 925°F 263 286 8.0 31.8 Ex. 1 1900°F 263 286 8.2 35.1 268 286 9.8 45.8 282 950°F 261 284 10.0 44.0 320 258 283 8.9 40.9 282 260 280 10.1 43.8 975°F 263 280 10.8 49.8 258 280 9.7 47.0 * * * * 900°F 259 285 * * 252 284 * * 270 292 7.6 34.4 925°F 271 294 7.6 35.4 Ex. 2 1900°F 267 289 9.0 41.0 272 292 8.9 37.8 950°F 274 290 11.0 47.0 262 283 9.5 46.6 975°F 264 283 10.2 46.6 227 259 279 11.5 50.3 239 -12- 2013355066 14 Oct 2016 267 285 10.6 47.6 233 250 265 11.3 56.7 — 925°F 248 262 11.4 58.2 — 250 265 12.5 58.9 — 245 258 10.9 56.1 384 Ex. A 1800°F 950°F 247 261 13.5 60.4 396 247 261 11.6 55.8 402 237 249 12.6 63.4 — 975°F 230 241 11.7 55.3 — 231 241 11.9 60.7 — 241 273 7.6 24.6 900°F 248 274 7.7 29.9 246 274 7.8 30.7 251 275 9.2 38.8 925°F 254 277 10.4 39.5 Ex. B 1900°F 247 273 9.2 41.1 252 277 9.6 42.6 950°F 259 281 8.5 35.2 244 277 9.1 39.6 241 270 9.0 42.7 975°F 244 266 11.3 53.3 249 272 10.8 50.4 Samples fractured in a manner such that valid results cou d not be obtained. TABLE IIB Heat Solution Age Y.S. U.T.S. %EI. %R.A. N.T.S. 241 272 8.4 30.2 900°F 237 272 8.0 30.4 243 272 8.1 29.6 244 273 9.5 36.8 925°F 239 274 9.8 37.4 Ex. C 1900°F 244 276 8.4 36.2 253 275 10.4 43.3 950°F 250 274 9.9 38.7 247 271 * 39.3 243 264 11.9 52.6 975°F 243 267 10.8 50.9 241 264 11.3 49.8 269 275 * * 925°F 274 293 6.0 27.5 * * * * Ex. D 1900°F 264 291 9.9 43.7 950°F 260 291 9.9 36.4 268 295 9.4 42.3 975°F 263 281 9.3 48.5 271 -13- 2013355066 14 Oct 2016 276 289 8.9 47.4 283 273 290 9.4 44.2 240 1000°F 251 269 11.6 59.0 252 270 11.5 54.6 250 275 11.4 54.5 270 295 3.6 9.4 925°F 274 295 4.5 10.6 271 293 8.7 34.6 276 296 8.0 42.1 950°F 270 290 8.7 40.8 280 295 7.4 34.4 Ex. E 1900°F * * * 975°F 268 291 8.5 43.5 269 287 8.7 43.5 257 272 10.6 49.9 1000°F 263 277 10.4 49.3 259 278 9.1 45.1 The results of Charpy V-notch (CVN) impact testing of Examples 1, 2, and D are shown in Table III below including the aging temperature, the Rockwell C-scale hardness (HRC), and the impact toughness (CVN) in foot-pounds. CVN testing was performed in accordance with ASTM Standard Test Procedure E23. 5 -14-

TABLE III

Example Age HRC CVN Avg. Ex. 1 950°F 54.0 4.4, 4.3, 3.8 4 Ex. 2 975°F 53.5 4.3, 4.4, 4.0 4 Ex. D 975°F 54.0 4.1,4.6, 3.7 4 2013355066 14 Oct 2016

Rising Step Load (RSL) samples for plane-strain fracture toughness testing and stress corrosion cracking resistance (SCC) were finish machined from the age-hardened bars of 5 Examples 1, 2, A, and D. Two samples from each heat were tested in air to provide a fracture toughness value (Kic). Additional samples were tested in 3.5% NaCl solution, natural pH, at room temperature, to provide a threshold stress intensity value (Kiscc).

Testing was performed on a test machine that meets the requirements of ASTM Standard Test Procedure E1290. The results of room temperature fracture toughness testing (Kic) and 10 stress corrosion cracking testing for Examples 1, 2, A, and D are presented in Table IV below including the plane-strain fracture toughness (Kic) in k si Vi n and the threshold stress intensity to produce stress corrosion cracking (Kiscc) in ksi Vin. Kiscc is reported for each step interval and as a final value. The lowest of the measured values for each example is designated as the final value of Kiscc in accordance with the standard test procedure. The tensile strength 15 values for each example are also reported in Table IV to show that the fracture toughness and stress corrosion cracking resistance were measured on alloys having similar levels of strength. -15- 2013355066 14 Oct 2016 TABLE IV Example Solution Age Avg. U.T.S. Kiscc Final Kiscc Kic 1 hour steps 2 hour steps 4 hour steps Ex. 1 1900°F 950°F 284 26.3 26.0 28.8 26 47.3, 46.0 Ex. 2 1900°F 975°F 282 29.0 22.0 34.8 22 45.5, 49.0 Ex. A 1800°F 950°F 260 71.6 32.3 36.0 32 90.5 Ex. D 1900°F 975°F 287 31.4 23.6 27.3 24 43.5, 42.1 -16- 2013355066 14 Oct 2016

Duplicate salt spray corrosion test cones were finish machined from the bars of Examples 1, 2, A, D after age-hardening. The cone samples were prepared by turning and hand polishing to a 600 grit finish. Prior to testing, all salt spray cones were passivated using 20% Nitric acid + 3 oz./gallon Sodium Dichromate at 120/140°F for 30 minutes. Samples were tested in accordance with ASTM B117, using a 5% NaCl concentration, natural pH, at 95°F for 200 hour test duration. Time to first rust was noted for all samples, as well as a final rating after the completion of 200 hours test duration. The results of the salt-spray testing are shown in Table V below including the time to first appearance of rust and a final rating after the completion of the test duration. The ratings are defined as follows: 1 = no rust, 2 = 1-3 rust spots, 3 = <5% rust, 4 = 5-10%, 5 = 10-20%, 6 = 20-40%, 7 = 40-60%, 8 = 60-80%, 9 = >80%.

TABLE V

Example Solution Age First Rust Final Rating Ex. 1 1900°F 950°F None, None 1,1 Ex. 2 1900°F 975°F None, None 1,1 Ex. A 1800°F 950°F None, None 1,1 Ex. D 1900°F 975°F None, None 1,1

Cyclic polarization (pitting) test samples were finish machined from the aged bars of Examples 1, 2, A, and D. Scans to measure pitting resistance were run on duplicate samples from each of those examples. The samples were tested in 3.5% NaCl solution, natural pH, at room temperature and were cleaned but not passivated prior to testing. Testing was performed with a modified ASTM Standard Test procedure G61 as described below.

Voltage values at the knee of the curve and protection potentials were measured for all samples. The results of the potentiodynamic pitting tests are shown in Table VI below including the pitting potential and the protection potential in millivolts (mV). - 17-

TABLE VI

Example Solution Age mV @ knee Protection Potential Ex. 1 1900°F 950°F 62.7, 66.7 11.1,34.9 Ex. 2 1900°F 975°F 76.2, 126.2 -12.7, -60.3 Ex. A 1800°F 950°F 76.2, 118.0 19.5, -8.7 Ex. D 1900°F 975°F 110.0, 126.2 -52.4, none 2013355066 14 Oct 2016 A steel article made from the alloy described above and processed in accordance with the foregoing processing steps provides a combination of properties that make it particularly useful for aircraft landing gear and other aircraft structural components, including but not limited to flap tracks and slat tracks, and for other applications where both high strength and corrosion resistance are required. In particular, a steel article fabricated from the alloy that is solution heat treated and age hardened as described above provides a tensile strength of at least 280 ksi and a fracture toughness (Kic) of at least 45 ksiVin when tested with a test machine that meets the requirements of ASTM Standard Test Procedure E1290. A steel article as described herein is also characterized by a Charpy V-notch impact energy of at least about 4 ft-lbs when tested in accordance with ASTM Standard Test Procedure E23. Further, a steel article as described herein is characterized by general corrosion resistance such that the article does not rust when tested in accordance with ASTM Standard Test procedure B 117 and by sufficient pitting corrosion resistance such that the article has a pitting potential of at least 62 mV when tested in accordance with a modified ASTM Standard Test procedure G61. The ASTM G61 test procedure was modified by using round bar rather than flat samples. The use of round bar samples exposes the end grains and can be considered to be a more severe test than the standard G61 procedure.

The terms and expressions which are employed in this specification are used as terms of description and not of limitation. There is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof. It is recognized that various modifications are possible within the invention described and claimed herein. - 18 - 2013355066 14 Oct 2016

The term ‘comprising’ as used in this specification and claims means ‘consisting at least in part of. When interpreting statements in this specification and claims which includes the ‘comprising’, other features besides the features prefaced by this term in each statement can also be present. Related terms such as ‘comprise’ and ‘comprised’ are to be interpreted in similar manner.

In this specification where reference has been made to patent specifications, other external documents, or other sources of information, this is generally for the purpose of providing a context for discussing the features of the invention. Unless specifically stated otherwise, reference to such external documents is not to be construed as an admission that such documents, or such sources of information, in any jurisdiction, are prior art, or form part of the common general knowledge in the art. - 19-

Claims

THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:

1. A precipitation hardenable, martensitic stainless steel alloy comprising in weight percent, about C 0.03 max Mn 1.0 max Si 0.75 max P 0.040 max S 0.0.005 max Cr 10 - 13 Ni 10.75-11.6 Mo 0.25 - 1.5 Cu 0.25 max Co 0.9-1.5 Ti 1.5-1.8 A1 0.4-0.8 Cb 0.3-0.8 B 0.010 max N 0.030 max and the balance is iron and usual impurities.
2. The alloy recited in Claim 1 which contains at least about 0.4% columbium.
3. The alloy recited in Claim 1 which contains at least about 10.5% chromium.
4. The alloy recited in Claim 1 which contains not more than about 12.5% chromium.
5. The alloy recited in Claim 1 which contains not more than about 1.7% titanium.
6. The alloy recited in Claim 1 which contains not more than about 1.25% molybdenum.
7. The alloy recited in Claim 1 which contains at least about 0.75 weight percent molybdenum.
8. The alloy recited in Claim 1 which contains up to about 0.003% calcium.
9. The alloy recited in Claim 1 which contains up to about 0.025% cerium.
10. A precipitation hardenable, martensitic stainless steel alloy comprising in weight percent, about C 0.02 max Mn 0.25 max Si 0.25 max P 0.015 max S 0.005 max Cr 10.5 - 12.5 Ni 10.75-11.25 Mo 0.75 - 1.25 Cu 0.25 max Co 0.9-1.25 Ti 1.5-1.7 A1 0.4-0.7 Cb 0.4 - 0.7 B 0.001 - 0.005 N 0.015 max and the balance is iron and usual impurities.
11. The alloy recited in Claim 10 which contains not more than about 1.1% cobalt.
12. The alloy recited in Claim 10 which contains at least about 10.85% nickel.
13. The alloy recited in Claim 10 which contains not more than about 0.6% columbium.
14. The alloy recited in Claim 10 which contains at least about 0.45% aluminum.
15. The alloy recited in Claim 10 which contains not more than about 0.65% aluminum.
16. The alloy recited in Claim 10 which contains at least about 0.9% molybdenum.
17. The alloy recited in Claim 10 which contains up to about 0.003% calcium.
18. The alloy recited in Claim 10 which contains up to about 0.025% cerium.
19. A precipitation hardenable, martensitic stainless steel alloy consisting essentially of, in weight percent, about C 0.015 max Mn 0.10 max Si 0.10 max P 0.010 max S 0.005 max Cr 11.0-12.0 Ni 10.85-11.25 Mo 0.9-1.1 Co 0.9-1.1 Cu 0.25 max Ti 1.5-1.7 A1 0.45-0.65 Cb 0.4-0.6 B 0.0015 - 0.0035 N 0.010 max and the balance is iron and usual impurities.
20. The alloy recited in Claim 19 which contains up to about 0.003% calcium.
21. The alloy recited in Claim 19 which contains up to about 0.025% cerium.