US3416916A - Ductile cobalt-base alloy - Google Patents

Ductile cobalt-base alloy Download PDF

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Publication number
US3416916A
US3416916A US563371A US56337166A US3416916A US 3416916 A US3416916 A US 3416916A US 563371 A US563371 A US 563371A US 56337166 A US56337166 A US 56337166A US 3416916 A US3416916 A US 3416916A
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United States
Prior art keywords
alloy
alloys
percent
cobalt
base alloy
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Expired - Lifetime
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US563371A
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English (en)
Inventor
Robert B Herchenroeder
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Carbide Corp
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Union Carbide Corp
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Filing date
Publication date
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Priority to US563371A priority Critical patent/US3416916A/en
Priority to SE10027/67*A priority patent/SE342474B/xx
Priority to DE1558676A priority patent/DE1558676B2/de
Priority to GB30501/67A priority patent/GB1137019A/en
Application granted granted Critical
Publication of US3416916A publication Critical patent/US3416916A/en
Anticipated expiration legal-status Critical
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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/07Alloys based on nickel or cobalt based on cobalt

Definitions

  • Another object of this invention is to provide a superior oxidation-resistant cobalt-base alloy in the form of wrought products.
  • a further object of this invention is to provide cobaltbase alloys that have an optimum combination of high strength and resistance to embrittlement and oxidation.
  • COnsistS essentially of about: 18 to 25 percent chromium, 11 to 15 percent tungsten, 1 6 to 25 percent nickel, 0.05 to 0.5 percent carbon, 0.001 to 0.025 percent boron balance cobalt and incidental impurities.
  • the alloy of this invention may contain the usual impurities found in commercial alloys of this class, i.e. up to, about percent iron, about 1.5 percent molybdenum, about 1 percent manganese, about 0.75 percent silicon; and about 0.15 percent total phosphorous, sulfur, hydrogen, oxygen, and nitrogen. Table 1 shows alloy ranges and specific compositions in accordance with the present invention.
  • alloys often called superalloys are especially suitable for service at high temperature except that they tend to embrittle after prolonged use at temperatures above about 1400" F.
  • each alloy has certain outstanding individual characteristics, none by itself has the advantage of combined optimum characteristics of high strength, oxidation resistance and resistance to embrittlement.
  • Alloy 1 is known to have outstanding, high temperature strength but its oxidation resistance is lower than that of Alloy 2.
  • Alloy 2 has outstanding oxidation resistance but its high temperature strength is lower than that of Alloy 1. Up to the present such limitations had to be tolerated in the application of these superalloys.
  • alloys of this invention provide an optimum combination of all the advantageous properties generally associated with this class of superalloys. As shown hereinbelow, the alloys of this invention have strengths equal to or higher than Alloy 1 and also have oxidation resistance characteristics approaching that of Alloy 2.
  • chromium within the ranges shown in Table 1, provides oxidation resistance and contributes to high temperature strength; chromium contents below the indicated range are not sufiicient to provide adequate oxidation resistance while chromium contents above the indicated range tend to yield alloys of decreased dutility at room temperature.
  • Tungsten is present in the alloy, within the indicated ranges, as a carbide former and in a solid solution matrix to provide high strength.
  • Molybdenum is not substitutable for tungsten in the alloy of this invention, although molybdenum may be present as an unavoidable impurity up to not more than 1.5 percent by weight in the total alloy as previously noted.
  • Carcon is required in the alloy within the range as indicated in Table 1 as a solid solution strengthening element and as a carbide former to provide high strength and nickel must be present in the alloy within the indicated ranges to provide adequate post aging ductility, oxidation resistance, and high temperature strength. Alloys containing less than 15.5 percent nickel tend to embrittle after prolonged use at temperatures between about 1400 F. and 1900 F.
  • Manganese may be present in the alloy in amounts not loys 1 and 2, in addition Table 6 shows that the alloys of this invention have much better oxidation resistance than alloy 1 of the prior art.
  • the oxidation tests of Table 6 were identical for all alloys tested. All oxidation test samples were nominally 0.07-inch thick sheet, 0.75-inch square and were uniformly polished to a 120-grit finish. One group of samples was exposed at 2000 F. for 100 hours continuously while another group was intermittently exposed at 2000 F. for eight 3-hour periods and four 19-hour periods for a total of 100 hours as indicated in Table 6. The oxidation rates were determined and are shown on the basis of mils penetration per year (m.p.y.). It is significant that the oxidation rates of the alloys of this invention closely approach those of alloy 2 which is generally recognized as the superior wrought oxidation-resistant alloy presently available in the metals industry.
  • Incidental impurities in amounts normally found in alloys of this type may be tolerated as previously mentioned while zirconium, columbium, titanium and tantalum, often added in alloys of this class, are not required in the alloys of this invention.
  • the combined total content in the final alloy of zirconium, columbium, titanium and tantalum must not exceed over one percent by weight, as impurities and residuals of prior processing steps, in order that the desired combination of properties be obtained.
  • alloys were prepared by a process commonly used in alloys of this class; however, other consolidating techniques could be used.
  • the alloy compositions were melted in an induction furnace, cast into ingots, forged and rolled into 0.063-inch thick sheet for testing purposes. Prior to testing, the alloys were annealed at 2150 F. for 15 minutes and fan cooled.
  • Compositions of alloys prepared and tested are given in Table 3.
  • the alloys of this invention described in Table 3 are in the range of about 19-20% Ni, 11-14% W, 19-22% Cr and 0.l-0.3% C. and will be seen to have an excellent combination of industrially useful properties. All of the alloys of Table 3, except alloy B, are in accordance with this invention. Tensile test results of these alloys, and prior are alloys, are shown in Table 4 while creep and stress-rupture test results are shown in Table 5.
  • the alloys of this invention are seen to be superior, or at least comparable to, both alloys 1 and 2 of the prior art.
  • the average tensile strengths of the alloys of this invention are about 1.5 times the strengths of al- TABLE 4.AVERAGE TENSILE PROPERTIES OF ALLOYS TESTED Yield Ultimate Strength Tensile Elongation, 0.2% Strength, Percent Offset, 1,000 1,000 p s l p.s.i.
  • a cobalt base alloy characterized by high temperah, oxidation resistance and resistance to em- DATA [.063-inch thick sheet] Load at Cup Depth, Cup Depth,
  • the two alloys are simi brittlement after exposure to elevated temperatures, said alloy consisting essentially of about:

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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)
  • Heat Treatment Of Strip Materials And Filament Materials (AREA)
  • Powder Metallurgy (AREA)
  • Manufacture Of Alloys Or Alloy Compounds (AREA)
US563371A 1966-07-07 1966-07-07 Ductile cobalt-base alloy Expired - Lifetime US3416916A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US563371A US3416916A (en) 1966-07-07 1966-07-07 Ductile cobalt-base alloy
SE10027/67*A SE342474B (fr) 1966-07-07 1967-06-30
DE1558676A DE1558676B2 (de) 1966-07-07 1967-06-30 Verwendung einer Kobalt-Legierung
GB30501/67A GB1137019A (en) 1966-07-07 1967-07-03 Cobalt base alloys

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US563371A US3416916A (en) 1966-07-07 1966-07-07 Ductile cobalt-base alloy

Publications (1)

Publication Number Publication Date
US3416916A true US3416916A (en) 1968-12-17

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US563371A Expired - Lifetime US3416916A (en) 1966-07-07 1966-07-07 Ductile cobalt-base alloy

Country Status (4)

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US (1) US3416916A (fr)
DE (1) DE1558676B2 (fr)
GB (1) GB1137019A (fr)
SE (1) SE342474B (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9377245B2 (en) 2013-03-15 2016-06-28 Ut-Battelle, Llc Heat exchanger life extension via in-situ reconditioning
US9435011B2 (en) 2013-08-08 2016-09-06 Ut-Battelle, Llc Creep-resistant, cobalt-free alloys for high temperature, liquid-salt heat exchanger systems
US9540714B2 (en) 2013-03-15 2017-01-10 Ut-Battelle, Llc High strength alloys for high temperature service in liquid-salt cooled energy systems
US9605565B2 (en) 2014-06-18 2017-03-28 Ut-Battelle, Llc Low-cost Fe—Ni—Cr alloys for high temperature valve applications
US9683280B2 (en) 2014-01-10 2017-06-20 Ut-Battelle, Llc Intermediate strength alloys for high temperature service in liquid-salt cooled energy systems
US9683279B2 (en) 2014-05-15 2017-06-20 Ut-Battelle, Llc Intermediate strength alloys for high temperature service in liquid-salt cooled energy systems
US10017842B2 (en) 2013-08-05 2018-07-10 Ut-Battelle, Llc Creep-resistant, cobalt-containing alloys for high temperature, liquid-salt heat exchanger systems

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2744010A (en) * 1951-02-12 1956-05-01 Gen Motors Corp High temperature co-cr alloys
US2746860A (en) * 1952-11-21 1956-05-22 Union Carbide And Carbodn Corp High temperature co-cr alloys
US2996379A (en) * 1958-12-04 1961-08-15 Union Carbide Corp Cobalt-base alloy
US3362816A (en) * 1963-06-22 1968-01-09 Fed Republic Of Germany Cobalt alloy

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2744010A (en) * 1951-02-12 1956-05-01 Gen Motors Corp High temperature co-cr alloys
US2746860A (en) * 1952-11-21 1956-05-22 Union Carbide And Carbodn Corp High temperature co-cr alloys
US2996379A (en) * 1958-12-04 1961-08-15 Union Carbide Corp Cobalt-base alloy
US3362816A (en) * 1963-06-22 1968-01-09 Fed Republic Of Germany Cobalt alloy

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9377245B2 (en) 2013-03-15 2016-06-28 Ut-Battelle, Llc Heat exchanger life extension via in-situ reconditioning
US9540714B2 (en) 2013-03-15 2017-01-10 Ut-Battelle, Llc High strength alloys for high temperature service in liquid-salt cooled energy systems
US10017842B2 (en) 2013-08-05 2018-07-10 Ut-Battelle, Llc Creep-resistant, cobalt-containing alloys for high temperature, liquid-salt heat exchanger systems
US9435011B2 (en) 2013-08-08 2016-09-06 Ut-Battelle, Llc Creep-resistant, cobalt-free alloys for high temperature, liquid-salt heat exchanger systems
US9683280B2 (en) 2014-01-10 2017-06-20 Ut-Battelle, Llc Intermediate strength alloys for high temperature service in liquid-salt cooled energy systems
US9683279B2 (en) 2014-05-15 2017-06-20 Ut-Battelle, Llc Intermediate strength alloys for high temperature service in liquid-salt cooled energy systems
US9605565B2 (en) 2014-06-18 2017-03-28 Ut-Battelle, Llc Low-cost Fe—Ni—Cr alloys for high temperature valve applications
US9752468B2 (en) 2014-06-18 2017-09-05 Ut-Battelle, Llc Low-cost, high-strength Fe—Ni—Cr alloys for high temperature exhaust valve applications

Also Published As

Publication number Publication date
GB1137019A (en) 1968-12-18
DE1558676C3 (fr) 1974-08-08
DE1558676B2 (de) 1974-01-17
DE1558676A1 (de) 1973-08-23
SE342474B (fr) 1972-02-07

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