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US3859147A - Hot hard stainless steel - Google Patents

Hot hard stainless steel Download PDF

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US3859147A
US3859147A US441499A US44149974A US3859147A US 3859147 A US3859147 A US 3859147A US 441499 A US441499 A US 441499A US 44149974 A US44149974 A US 44149974A US 3859147 A US3859147 A US 3859147A
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stainless steel
hardness
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hot
alloy
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Thoni V Philip
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Carpenter Technology Corp
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium with vanadium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten

Definitions

  • ABSTRACT A hot hard chromium stainless steel having good hot workability containing about 0.91.4% carbon, 13-19% chromium, 1.52.75% molybdenum, 0.32.5% vanadium, O.100.55% columbium and the balance primarily iron.
  • This invention relates to stainless steel and, more particularly, to a stainless steel having good hot workability, which can be heat treated to high hardnesses, and which in its heat treated condition has good wear resistance and a high degree of hot hardness at elevated temperatures.
  • A.I.S.I. Type 440C stainless steel contains about 0.95-1 .20% carbon, a maximum of 1.00% each of manganese and silicon, 16.00-18.00% chromium, a maximum of 0.75% molybdenum and the balance iron except for incidental impurities.
  • Type 440C has long been used in the manufacture of such parts as stainless bearings for use at room temperature (e.g. 70F). The steel has good forgeability, but because of its relatively low hot hardness cannot be used to make parts which in use must withstand loads at elevated temperatures.
  • Alloy A has a much higher hot hardness than Type 440 C and good corrosion resistance, but it is very difficult to hot work.
  • Alloys B and C have been reported as having even higher hot hardness than Alloy A, and Alloy D was developed for making bearings intended for use at elevated temperatures.
  • the hot workability of Alloys A-D decreases with increasing alloy content so that Alloy D with the maximum alloy content has the poorest hot workability and the lowest ingot yield.
  • a further object of this invention is to provide such a stainless steel having high hot hardness and good temper resistance combined with good hot workability so that it is eminently well suited for use in making parts intended for use in corrosive environments both at room and elevated temperatures such as bearing parts, cams, shafts, gears, gage blocks, micrometer spindles and others.
  • the remainder of the alloy is iron except for incidental impurities which may vary from a few hundredths of a percent or less as in the case of sulfur and phosphorus or up to 1 or 2 tenths of a percent as in the case of a deoxidizer such as aluminum or a few hundredths of a percent as in the case of calcium so long as the desired properties of the alloy are not impaired.
  • incidental impurities may vary from a few hundredths of a percent or less as in the case of sulfur and phosphorus or up to 1 or 2 tenths of a percent as in the case of a deoxidizer such as aluminum or a few hundredths of a percent as in the case of calcium so long as the desired properties of the alloy are not impaired.
  • 1t is to be noted that while the best all-round properties are provided by the preferred composition, it is not intended to restrict the'ranges indicated by presenting them in tabular form for ready reference. It is contemplated that any one or more of the preferred ranges indicated can be used with any one
  • a minimum of about 0.9% carbon is required to ensure the attainment of the minimum desired hardness of no less than about Rc 60. Carbon ranging from about 0.95-l.15% is preferred. As the carbon content approaches 1.4%, increasing difficulty is experienced in forging unless the carbideforming elements, chromium, molybdenum, vanadium and columbium, are balanced toward the lower ends of their permitted ranges.
  • chromium is present in an amount ranging from about 13.5-14.5% because above about 14.5% chromium, increasing difficulty is encountered in forging the alloy unless such elements as molybdenum, vanadium and carbon are reduced toward the lower end of their ranges.
  • Molybdenum in amounts of about 3% or more contributes to the difficulty hitherto encountered in such well-known modifications of Type 440C as Alloy A. Therefore, molybdenum is limited to a maximum of about 2.75% and preferably to no more than about 2.5%. Below about 1.5%, molybdenum is not present in a sufficient amount to contribute sufficiently to the secondary hardening reaction by which the alloy attains the desired as-heat-treated hardness.
  • Vanadium contributes to the forgeability, heattreated hardness, and hot hardness of this alloy. Below about 0.3% vanadium is not present in a sufficient amount for this purpose. Preferably 0.75-1.25% vanadium is used to provide the best combination of both forgeability and hardness. For best as-heat-treated hardness, the larger amounts of vanadium are used, that is up to about 2.5%. However, substantially better forgeability is obtained with only a maximum of about 2% vanadium and with no significant reduction in hot hardness. With up to 2% vanadium, up to 1.2% carbon is preferably used, and, with vanadium in excess of 2%, carbon in excess of 1.2% is preferably used.
  • columbium In the absence of vanadium, columbium has either a negligible effect on the heat-treated hardness or, when larger amounts of columbium are used, some slight reduction in the as-heat-treated hardness results. Apparently columbium does not contribute to the secondary hardening effect in this composition. However, a small addition of columbium, about 0.100.55%, preferably 0.200.35% makes possible the use of a higher austenitizing temperature to provide a better secondary hardness rather than the deleterious effect which would normally be expected from using austenitizing temperatures as high as about 2100F. Above about 0.55% columbium some deleterious effect on required properties, such as fatigue life, is to be expected without any compensatory improvement in other properties.
  • the alloy is melted and cast into ingots in the usual way, and, because of its exceptional hot workability, it is readily worked into parts using conventional techniques.
  • the alloy is preferably forged from a furnace temperature of about 2000 to 2050F.
  • Annealing is preferably carried out at about 1550 to 1650F.
  • the preferred annealing treatment consists of thoroughly heating at 1600F, then cooling at the rate of about 20/hr. to about 1450F where the part is held for about 2 to 4 hours, then cooling at the rate of about 20/hr. to about 1350F where it is again held for about 2 to 4 hours, then again cooling at the rate of 20/hr. down to 1 100F or below, and then cooling in air.
  • Austenitizing is carried out at about 2050 to 2150F, preferably at about 2100F, followed by oil quenching and refrigerating at lF or below.
  • the parts are preferably stress relieved by heating at about 300-350F to avoid warping and possible cracking. It is an advantageous characteristic of this allow that no more of a tempering treatment is required to develope its full room temperature and hot hardness than two successive 2 hour heat treatments at the desired temperature with intermediate cooling.
  • the parts, following the first stage of the tempering treatment are cooled to room temperature and then refrigerated at about -l05F or below to ensure maximum freedom from retained austenite, but this refrigeration is not required to develope full room temperature and hot hardness.
  • the alloy of this invention is balanced so that in its heat treated condition it is substantially free of retained austenite, that is, hardened and tempered parts contain no more than about 3%, preferably no more than 1%, retained austenite.
  • EXAMPLE 1 As an example of the present invention, a -pound air induction heat was prepared having the following analysis:
  • the remainder of the ingot was forged from 2200F by pressing to a 2 inch round cornered square bar which was then hot cut into three substantially equal lengths. Two of these lengths were reheated, and one was then forged to a 1% inch octagonal bar and the other to a 1% inch square bar. Forging was considered very easy and was carried out without any defects such as split ends or surface tears.
  • the bars were again annealed, and the annealed hardness was found to be Rc 29.5. When the bars were annealed using the preferred annealing cycle with an initial temperature of 1560F where they were held for 4 hours, the resulting hardness was Rb 100.
  • Specimens of the alloy which had been annealed using the last mentioned preferred cycle were then austenitized at 2050 and 2100F, oil quenched, refrigerated at about -F and then tempered at 975F, 1000F and 1025F.
  • Each tempering treatment included heating at temperature for 2 hours, air cooling to room temperature, refrigerating at about 105F until thoroughly cooled to that temperature then holding at the tempering temperature one more for 2 hours, and then air cooling. The results are shown in Table 111.
  • the hot hardnesses in Table V are exemplary of this alloy which consistently provides a minimum hot hardness of Rc 50 at 1000F following the two stage tempering with intermediate cooling at least to room temperature.
  • the alloy of this invention is well suited for use in making parts which are required to withstand loading at temperatures ranging from about 350 to 1000F.
  • a stainless steel having good hot workability which is hardened by heating at about 2100F and tempered to a room temperature hardness of at least about Rockwell C60 and a hot hardness greater than about Re 50 at 1000F, and which in its heat treated condition is substantially free of retained austenite, which by weight consists essentially of about Carbon 0.9-1.4% Manganese 1% Maximum Silicon 1% Maximum Chromium 13-19% Molybdenum l.52.75% Vanadium 0.3-2.5% Columbium 0.100.55%
  • the balance being essentially iron and incidental impurities.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)

Abstract

A hot hard chromium stainless steel having good hot workability containing about 0.9-1.4% carbon, 13-19% chromium, 1.5-2.75% molybdenum, 0.3-2.5% vanadium, 0.10-0.55% columbium and the balance primarily iron.

Description

United States Patent 1191 Philip 1 Jan.7, 1975 HOT HARD STAINLESS STEEL [75] Inventor: Thoni V. Philip, Reading, Pa.
[73] Assignee: Carpenter Technology Corporation,
Reading, Pa.
22 Filed: Feb. 11, 1974 21 Appl. No.: 441,499
Related US. Application Data [63] Continuation-impart of Ser. No. 233,804, March 10,
1972, abandoned.
[52] US. Cl. 148/37, 75/126 B, 75/126 E, 75/126 F, 75/130.5, 148/135 [51] Int. Cl. C22c 39/14 [58] Field 01' Search 148/37, 135; 75/126 B, 75/126 E, 126 F, 126 R, 130.5
[56] References Cited UNITED STATES PATENTS 2,199,096 4/1940 Berglund 148/37 2,225,730 12/1940 Armstrong 148/37 2,228,106 1/1941 Beria 148/37 2,789,049 4/1957 DeLong et a1. 75/126 E 2,934,430 4/1960 Klaybor et a1. 148/37 3,069,257 12/1962 Clarke 148/37 3,139,337 6/1964 Boyle et a1... 75/126 E 3,167,423 l/l965 Johnson 75/126 E 3,257,200 6/1966 Hodge 75/126 E 3,660,174 5/1972 Jakenberg 1 148/37 FOREIGN PATENTS OR APPLICATIONS 733,146 7/1955 Great Britain 75/126 E Primary ExaminerWalter R. Satterfield Attorney, Agent, or Firm-Edgar N. Jay
[57] ABSTRACT A hot hard chromium stainless steel having good hot workability containing about 0.91.4% carbon, 13-19% chromium, 1.52.75% molybdenum, 0.32.5% vanadium, O.100.55% columbium and the balance primarily iron.
7 Claims, No Drawings HOT HARD STAINLESS STEEL RELATED CASES This application is a continuation-in-part of my copending application Ser. No. 233,804, and now abandoned, filed Mar. 10, 1972.
BACKGROUND OF THE INVENTION This invention relates to stainless steel and, more particularly, to a stainless steel having good hot workability, which can be heat treated to high hardnesses, and which in its heat treated condition has good wear resistance and a high degree of hot hardness at elevated temperatures.
A.I.S.I. Type 440C stainless steel contains about 0.95-1 .20% carbon, a maximum of 1.00% each of manganese and silicon, 16.00-18.00% chromium, a maximum of 0.75% molybdenum and the balance iron except for incidental impurities. Type 440C has long been used in the manufacture of such parts as stainless bearings for use at room temperature (e.g. 70F). The steel has good forgeability, but because of its relatively low hot hardness cannot be used to make parts which in use must withstand loads at elevated temperatures. Some stainless steels having higher hot hardness than Type 440C which have been developed as modifications of that type are set forth in Table I.
In each alloy, the balance is iron except for incidental impurities. Alloy A has a much higher hot hardness than Type 440 C and good corrosion resistance, but it is very difficult to hot work. Alloys B and C have been reported as having even higher hot hardness than Alloy A, and Alloy D was developed for making bearings intended for use at elevated temperatures. Unfortunately, the hot workability of Alloys A-D decreases with increasing alloy content so that Alloy D with the maximum alloy content has the poorest hot workability and the lowest ingot yield. The poorer hot workability and reduced yields attained in the manufacture of wrought products from Alloys A-D as compared to Type 440C results in parts fabricated of Alloys A-D being costlier than those made from 440C with the cost increasing disproportionately to the increase in alloying content.
SUMMARY OF THE INVENTION It is therefore a principal object of this invention to provide a stainless steel having greatly improved wear resistance, hot hardness and temper resistance as compared to Type 440C alloy, but which is characterized by a hot workability equivalent to that of Type 440C and is free of the difficulties associated with other modifications of Type 440C.
A further object of this invention is to provide such a stainless steel having high hot hardness and good temper resistance combined with good hot workability so that it is eminently well suited for use in making parts intended for use in corrosive environments both at room and elevated temperatures such as bearing parts, cams, shafts, gears, gage blocks, micrometer spindles and others.
Much of the foregoing objects as well as further advantages of this invention are attained by providing a stainless steel which consists essentially of the following broad analysis while all of the objects and advantages are provided by the stainless steel which consists essentially of the following preferred analysis, both in the approximate amounts indicated in weight percent in keeping with good metallurgical practice:
The remainder of the alloy is iron except for incidental impurities which may vary from a few hundredths of a percent or less as in the case of sulfur and phosphorus or up to 1 or 2 tenths of a percent as in the case of a deoxidizer such as aluminum or a few hundredths of a percent as in the case of calcium so long as the desired properties of the alloy are not impaired. 1t is to be noted that while the best all-round properties are provided by the preferred composition, it is not intended to restrict the'ranges indicated by presenting them in tabular form for ready reference. It is contemplated that any one or more of the preferred ranges indicated can be used with any one or more of the broad ranges indicated for the remaining elements.
DESCRIPTION or THE PREFERRED EMBODIMENTS In the alloy of this invention, a minimum of about 0.9% carbon is required to ensure the attainment of the minimum desired hardness of no less than about Rc 60. Carbon ranging from about 0.95-l.15% is preferred. As the carbon content approaches 1.4%, increasing difficulty is experienced in forging unless the carbideforming elements, chromium, molybdenum, vanadium and columbium, are balanced toward the lower ends of their permitted ranges.
A minimum of about 13% chromium is required to provide the desired corrosion resistance particularly to the environment usually to be encountered in jet engines under operating conditions, including water vapor, chloride ions and other corrodents to be found in the atmosphere. Preferably chromium is present in an amount ranging from about 13.5-14.5% because above about 14.5% chromium, increasing difficulty is encountered in forging the alloy unless such elements as molybdenum, vanadium and carbon are reduced toward the lower end of their ranges.
Molybdenum in amounts of about 3% or more contributes to the difficulty hitherto encountered in such well-known modifications of Type 440C as Alloy A. Therefore, molybdenum is limited to a maximum of about 2.75% and preferably to no more than about 2.5%. Below about 1.5%, molybdenum is not present in a sufficient amount to contribute sufficiently to the secondary hardening reaction by which the alloy attains the desired as-heat-treated hardness.
Vanadium contributes to the forgeability, heattreated hardness, and hot hardness of this alloy. Below about 0.3% vanadium is not present in a sufficient amount for this purpose. Preferably 0.75-1.25% vanadium is used to provide the best combination of both forgeability and hardness. For best as-heat-treated hardness, the larger amounts of vanadium are used, that is up to about 2.5%. However, substantially better forgeability is obtained with only a maximum of about 2% vanadium and with no significant reduction in hot hardness. With up to 2% vanadium, up to 1.2% carbon is preferably used, and, with vanadium in excess of 2%, carbon in excess of 1.2% is preferably used.
In the absence of vanadium, columbium has either a negligible effect on the heat-treated hardness or, when larger amounts of columbium are used, some slight reduction in the as-heat-treated hardness results. Apparently columbium does not contribute to the secondary hardening effect in this composition. However, a small addition of columbium, about 0.100.55%, preferably 0.200.35% makes possible the use of a higher austenitizing temperature to provide a better secondary hardness rather than the deleterious effect which would normally be expected from using austenitizing temperatures as high as about 2100F. Above about 0.55% columbium some deleterious effect on required properties, such as fatigue life, is to be expected without any compensatory improvement in other properties.
This alloy is melted and cast into ingots in the usual way, and, because of its exceptional hot workability, it is readily worked into parts using conventional techniques. The alloy is preferably forged from a furnace temperature of about 2000 to 2050F. Annealing is preferably carried out at about 1550 to 1650F. The preferred annealing treatment consists of thoroughly heating at 1600F, then cooling at the rate of about 20/hr. to about 1450F where the part is held for about 2 to 4 hours, then cooling at the rate of about 20/hr. to about 1350F where it is again held for about 2 to 4 hours, then again cooling at the rate of 20/hr. down to 1 100F or below, and then cooling in air. Austenitizing is carried out at about 2050 to 2150F, preferably at about 2100F, followed by oil quenching and refrigerating at lF or below. Before this refrigeration, the parts are preferably stress relieved by heating at about 300-350F to avoid warping and possible cracking. It is an advantageous characteristic of this allow that no more of a tempering treatment is required to develope its full room temperature and hot hardness than two successive 2 hour heat treatments at the desired temperature with intermediate cooling. Preferably, in addition to cooling to room temperature, the parts, following the first stage of the tempering treatment, are cooled to room temperature and then refrigerated at about -l05F or below to ensure maximum freedom from retained austenite, but this refrigeration is not required to develope full room temperature and hot hardness.
It is to be noted that the alloy of this invention is balanced so that in its heat treated condition it is substantially free of retained austenite, that is, hardened and tempered parts contain no more than about 3%, preferably no more than 1%, retained austenite.
EXAMPLE 1 As an example of the present invention, a -pound air induction heat was prepared having the following analysis:
Weight percent Carbon 1.07 Manganese 0.3) Silicon 0.25 Chromium 14.22 Molybdenum 2.19 Vanadium 0.99 Columbium 0.27
TABLE II ,Impact Strength Test Temp. "F (Ft. lbs) El. R.A.
These results, particularly the ductility as measured by the percent elongation, clearly demonstrate the improved forgeability of this alloy, particularly as compared to the aforementioned Alloys A-D. In fact, the forgeability of this alloy is not significantly different from that of Type 440C.
The remainder of the ingot was forged from 2200F by pressing to a 2 inch round cornered square bar which was then hot cut into three substantially equal lengths. Two of these lengths were reheated, and one was then forged to a 1% inch octagonal bar and the other to a 1% inch square bar. Forging was considered very easy and was carried out without any defects such as split ends or surface tears. The bars were again annealed, and the annealed hardness was found to be Rc 29.5. When the bars were annealed using the preferred annealing cycle with an initial temperature of 1560F where they were held for 4 hours, the resulting hardness was Rb 100.
Specimens of the alloy which had been annealed using the last mentioned preferred cycle were then austenitized at 2050 and 2100F, oil quenched, refrigerated at about -F and then tempered at 975F, 1000F and 1025F. Each tempering treatment included heating at temperature for 2 hours, air cooling to room temperature, refrigerating at about 105F until thoroughly cooled to that temperature then holding at the tempering temperature one more for 2 hours, and then air cooling. The results are shown in Table 111.
TABLE 111 Hardness (Re) Tempering Specimens tempered at 975 and 1025F were examined for retained austenite but none could be detected.
The resistance of this alloy to tempering is even better demonstrated by the following results obtained when specimens of the alloy were austenitized at 2100F for minutes, oil quenched, refrigerated at 105F, and then tempered for 1 hour at the temperatures indicated in Table IV. In the regrigerated condition, the specimens had a hardness of Re 64.0. For comparison, typical specimens of Type 440C alloy which had been austenitized at 1950F for minutes, oil quenched and refrigerated at 105F were also tempered for 1 hour at the temperatures indicated in Table IV with the results shown. The refrigerated hardness of To demonstrate the hot hardness of the alloy, specimens were machined from the 1% inch square bar and were preheated at 1500F, austenitized at 2100F, step quenched in a salt bath to 1000F, air cooled, refrigerated at l05F, and then tempered by heating at 975F for 2 hours, refrigerated and once again heating at 975F for 2 hours. Hardnesses were measured at room temperature, 500F, 600F, 700F, 800F, 900F, 1000F with the following results.
TABLE V HARDNESS (Re) Room 500 600 700 800 900 1000 61.5 58.5 57.3 55.4 54.8 52.9 61.5 57.8 56.7 55.5 54.5 52.5
The hot hardnesses in Table V are exemplary of this alloy which consistently provides a minimum hot hardness of Rc 50 at 1000F following the two stage tempering with intermediate cooling at least to room temperature.
Because of its unique combination of heattreated hardness, hot hardness, temper resistance, wear resistance and corrosion resistance, with good forgeability, the alloy of this invention is well suited for use in making parts which are required to withstand loading at temperatures ranging from about 350 to 1000F.
The terms and expressions which have been employed are used as terms of description and not of limitation, and 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, but it is recognized that various modifications are possible within the scope of the invention claimed.
What is claimed is:
1. A stainless steel having good hot workability, which is hardened by heating at about 2100F and tempered to a room temperature hardness of at least about Rockwell C60 and a hot hardness greater than about Re 50 at 1000F, and which in its heat treated condition is substantially free of retained austenite, which by weight consists essentially of about Carbon 0.9-1.4% Manganese 1% Maximum Silicon 1% Maximum Chromium 13-19% Molybdenum l.52.75% Vanadium 0.3-2.5% Columbium 0.100.55%
the balance being essentially iron and incidental impurities.
2. The stainless steel set forth in claim 1 which contains about O.95-1.l5% carbon.
3. The stainless steel set forth in claim 2 which contains about 13.514.5% chromium.
4. The stainless steel set forth in claim 3 which contains about 1.752.5% molybdenum.
5. The stainless steel set forth in claim 4 which contains about 0.75l.25% vanadium.
6. The stainless steel set forth in claim 5 which contains about 0.20-0.35% columbium.
7. The stainless steel set forth in claim 6 which contains less than about 1% retained austenite.

Claims (7)

1. A STAINLESS STEEL HAVING GOOD HOT WORKABILITY, WHICH IS HARDENED BY HEATING AT ABOUT 2100*F AND TEMPERED TO A ROOM TEMPERATURE HARDNESS OF AT LEAST ABOUT ROCKWELL C60 AND A HOT HARDNESS GREATER THAN ABOUT RC 50 AT 1000*F, AND WHICH IN ITS HEAT TREATED CONDITION IS SUBSTANTIALLY FREE OF RETAINED AUSTENITE, WHICH BY WEIGHT CONSISTS ESSENTIALLY OF ABOUT CARBON 0.9-1.4% MANGANESE 1% MAXIMUM SILCON 1% MAXIMUM CHROMIUM 13-19% MOLBDENUM 1.5-2.75% VANADIUM 0.3-2.5% COLUMBIUM 0.10-0.55% THE BALANCE BEING ESSENTIALLY IRON AND INCIDENTAL IMPURITIES.
2. The stainless steel set forth in claim 1 which contains about 0.95-1.15% carbon.
3. The stainless steel set forth in claim 2 which contains about 13.5-14.5% chromium.
4. The stainless steel set forth in claim 3 which contains about 1.75-2.5% molybdenum.
5. The stainless steel set forth in claim 4 which contains about 0.75-1.25% vanadium.
6. The stainless steel set forth in claim 5 which contains about 0.20-0.35% columbium.
7. The stainless steel set forth in claim 6 which contains less than about 1% retained austenite.
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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4150978A (en) * 1978-04-24 1979-04-24 Latrobe Steel Company High performance bearing steels
US4325758A (en) * 1980-10-02 1982-04-20 Western Electric Company, Inc. Heat treatment for high chromium high carbon stainless steel
EP0295111A2 (en) * 1987-06-11 1988-12-14 Aichi Steel Works, Ltd. A steel having good wear resistance
US4985092A (en) * 1987-06-11 1991-01-15 Aichi Steel Works, Limited Steel having good wear resistance
FR2654115A1 (en) * 1989-11-07 1991-05-10 Thyssen Edelstahlwerke Ag IMPLEMENTING A CHROME MARTENSITIC STEEL FOR MEAT GRINDER KNIVES.
US5674449A (en) * 1995-05-25 1997-10-07 Winsert, Inc. Iron base alloys for internal combustion engine valve seat inserts, and the like
EP0799902A1 (en) * 1994-10-13 1997-10-08 Hitachi Metals, Ltd. Piston ring material excellent in workability
US5944920A (en) * 1996-04-10 1999-08-31 Hitachi Metals, Ltd. Piston ring material excellent in workability
US20060283526A1 (en) * 2004-07-08 2006-12-21 Xuecheng Liang Wear resistant alloy for valve seat insert used in internal combustion engines
US20070187458A1 (en) * 2006-02-16 2007-08-16 Stoody Company Stainless steel weld overlays with enhanced wear resistance
US20110162520A1 (en) * 2010-01-05 2011-07-07 Smc Kabushiki Kaisha Linear actuator
US20110162519A1 (en) * 2010-01-05 2011-07-07 Smc Kabushiki Kaisha Linear actuator
CN102213246A (en) * 2010-04-07 2011-10-12 Smc株式会社 Linear actuator

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US20110162520A1 (en) * 2010-01-05 2011-07-07 Smc Kabushiki Kaisha Linear actuator
US20110162519A1 (en) * 2010-01-05 2011-07-07 Smc Kabushiki Kaisha Linear actuator
US8955424B2 (en) 2010-01-05 2015-02-17 Smc Kabushiki Kaisha Linear actuator
CN102213246A (en) * 2010-04-07 2011-10-12 Smc株式会社 Linear actuator
US20110247487A1 (en) * 2010-04-07 2011-10-13 Smc Kabushiki Kaisha Linear actuator
US8939064B2 (en) * 2010-04-07 2015-01-27 Smc Kabushiki Kaisha Linear actuator
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