US3399058A - Sulfidation and oxidation resistant cobalt-base alloy - Google Patents
Sulfidation and oxidation resistant cobalt-base alloy Download PDFInfo
- Publication number
- US3399058A US3399058A US617755A US61775567A US3399058A US 3399058 A US3399058 A US 3399058A US 617755 A US617755 A US 617755A US 61775567 A US61775567 A US 61775567A US 3399058 A US3399058 A US 3399058A
- Authority
- US
- United States
- Prior art keywords
- cobalt
- sulfidation
- alloy
- yttrium
- alloys
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910045601 alloy Inorganic materials 0.000 title description 73
- 239000000956 alloy Substances 0.000 title description 73
- 238000005486 sulfidation Methods 0.000 title description 31
- 230000003647 oxidation Effects 0.000 title description 23
- 238000007254 oxidation reaction Methods 0.000 title description 23
- 239000002585 base Substances 0.000 description 35
- 229910052727 yttrium Inorganic materials 0.000 description 28
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 26
- 239000000203 mixture Substances 0.000 description 22
- 229910052782 aluminium Inorganic materials 0.000 description 19
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 19
- 238000012360 testing method Methods 0.000 description 13
- 239000010941 cobalt Substances 0.000 description 12
- 229910017052 cobalt Inorganic materials 0.000 description 12
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 12
- 239000007789 gas Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 238000002485 combustion reaction Methods 0.000 description 8
- 150000002739 metals Chemical class 0.000 description 8
- 239000010955 niobium Substances 0.000 description 8
- 229910052715 tantalum Inorganic materials 0.000 description 8
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 8
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 8
- 229910052721 tungsten Inorganic materials 0.000 description 8
- 239000010937 tungsten Substances 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 229910052750 molybdenum Inorganic materials 0.000 description 7
- 239000011733 molybdenum Substances 0.000 description 7
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 239000011593 sulfur Substances 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 6
- 239000011651 chromium Substances 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 239000000446 fuel Substances 0.000 description 6
- -1 alkaline-earth metal salts Chemical class 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 208000016261 weight loss Diseases 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- 229910000531 Co alloy Inorganic materials 0.000 description 3
- 229910001026 inconel Inorganic materials 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910052692 Dysprosium Inorganic materials 0.000 description 1
- 229910052691 Erbium Inorganic materials 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910001122 Mischmetal Inorganic materials 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910052769 Ytterbium Inorganic materials 0.000 description 1
- 229910002065 alloy metal Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- KBQHZAAAGSGFKK-UHFFFAOYSA-N dysprosium atom Chemical compound [Dy] KBQHZAAAGSGFKK-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 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 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/07—Alloys based on nickel or cobalt based on cobalt
Definitions
- ABSTRACT OF THE DISCLOSURE A sulfidation and oxidation resistant cobalt-base alloy comprised of a major amount of cobalt, between about 0.05% and 3.0% by weight yttrium, between about 1.0% and 6.0% by weight aluminum and preferably also containing chromium, tungsten and/ or molybdenum, columbium and/ or tantalum and carbon.
- This invention relates generally to metal alloys and more particularly to alloys provided for use in the manufacture of machine parts, such as gas turbine wheels and/or blades, and nozzle vanes, which are exposed to high-temperature combustion gases containing oxygen, sulfur, lead, and/ or other chemicals that cause oxidation, sulfidation, corrosion and other deleterious effects.
- Sulfidation is a metal deterioration which takes place particularly in the heated sections of gas turbines which are exposed to gaseous combustion products of sulfur and/ or lead containing fuels such as fuel oil, diesel fuel, aviation gasoline and the like.
- the problem is especially serious under desert or salt water atmosphere conditions where the presence of alkali or alkaline-earth metal salts such as sodium chloride, even in concentrations as low as 0.1 part per million, are found to catalyze the sulfidation reaction.
- high-temperature metallurgy for use in oxygen containing environments has been limited to: (1) nickel-base alloys which, although oxidation resistant to 2000 F. are not satisfactory in sulfur containing atmospheres over 1650 especially when alkali and alkalineearth metal salts are present, or over 1750 F. when lead deposits are present; and (2) cobalt-base alloys which are resistant to sulfidation and lead attack up to 1850 F. but are not resistant to oxidation above 1750 F.
- One aim of this invention is to provide an alloy having an equal or better oxidation resisting quality than the high strength nickel-base alloys, such as the alloy known as Inconel 713C, and an equal or better sulfidation resisting quality than the cobalt-base alloys, such as that identified by the trademark WI52.
- An object of this invention is to provide an alloy having high resistance to oxidation, sulfidation and lead corrosion when exposed, in oxygen containing environments, to gaseous products of combustion at about 2000 F. temperatures, such as are produced by burning JP4 or other gas turbine fuels.
- Still another object of the invention is to provide a cobalt-base alloy having a maximum of about 6.0 weight percent aluminum and a maximum of about 3.0 weight percent yttrium to further increase the resistance of the alloy to oxidation, sulfidation and lead corrosion when exposed to an atmosphere containing combustion products of fuels of the type employed to operate gas turbine engines.
- the superior alloys of this invention are cobalt-base alloys containing a small amount of yttrium and aluminum and preferably a number of other metals which will improve the strength properties of the material.
- cobalt-base alloy as used herein and as understood in the art, is meant a metallic composition wherein the major element present in cobalt and preferably wherein the cobalt is present in a major amount. More specifically it has been found according to the invention cobalt-base alloys containing from about 0.05 to about 3.0% by weight yttrium and from about 1.0 to about 6.0% by weight aluminum possess outstanding sulfidation and oxidation deterioration resistance.
- the cobalt-base alloys of the invention contain between about 50% and 65% cobalt.
- the composition is also necessary for the composition to contain tungsten and/or tantalum wherein the total amount of this group of metals is between about 3% and 20% by weight of the alloy composition.
- the preferred amounts of these metals individually are between 0% and 15% and more preferably between about 4% and 10% individually for tungsten and tantalum with the total amount of this group of metals being no more than about 20% by weight of the alloy composition.
- molybdenum may be present to replace all or part of the tungsten and columbium may be present to replace a part or all of the tantalum.
- Molybdenum preferably may be present up to about 10% and columbium up to about 2.0% by weight of the alloy composition. It is also desirable to have chromium present in order to provide a higher strength alloy for many uses. Thus, amounts of chromium up to about 25% and preferably between about 10% and about 25% may be used. The presence of a small amount of carbon also increases the strength of the alloy. However, where the carbon content gets above about 0.5% by Weight oxidation corrosion resistance may be sacrificed somewhat. Thus, suitable carbon concentrations are between about 0.05% and about 0.5% by Weight.
- a convenient way to express the concentrations of the preferred cobalt-base alloys of this invention is by mole ratios based on cobalt.
- the preferred alloy composi- Patented Aug. 27, 1968 .tions corresponding to the concentrations as set forth above are as follows:
- the yttrium used in the alloys of the invention may be pure or may be added as a yttrium composition referred to as a misch metal containing at least about 70% yttrium and a small amount of other elements such as lanthanum, cerium, neodymium, Samarium, gadolinium, dysprosium, erbium, ytterbium, etc., as Well as copper, calcium, magnesium, silicon and the like.
- a yttrium composition referred to as a misch metal containing at least about 70% yttrium and a small amount of other elements such as lanthanum, cerium, neodymium, Samarium, gadolinium, dysprosium, erbium, ytterbium, etc., as Well as copper, calcium, magnesium, silicon and the like.
- Example I In carrying out the present invention, one of the presently available cobalt alloys, identified as WI-52 and having the following analysis:
- a graph is shown in FIG. 1 having curves to indicate the results of the tests. As shown in the upper left-hand corner of FIG. 1, the following symbols are used to identify the alloys and the curves plotted to illustrate the effect of the test thereon. It will be apparent from the graph that the cobalt alloy WI-SZ, modified to include small portions of both yttrium and aluminum, gained less weight and was therefore more oxidation resistant than the unmodified cobalt-base alloy or the alloy modified by the addition of either of the elements alone. The graph also shows that the alloy WI52 modified by the addition of 1% yttrium and 3% aluminum (designated X) 'has oxidation resisting qualities equal to the nickel-base alloy.
- Example II Test samples of the modified cobalt-base alloy X were subjected to sulfidation resistance tests which. were run in an environment consisting of the combustion products of JP4 fuel (CO N 0 H O, S0 at elevated temperatures. After completion of the test the samples are cleaned by boiling in concentrated HNO and wire brushed. The cleaned samples are then weighed to determined any weight change. The results of such tests were compared with the results of similar tests made on the alloy WI-52 without modification and with the addition of a small part of yttrium alone.
- a chart, identified as FIG. 2 in the drawings, shows the increased resistance to sulfidation secured by the addition of similar small percentages of aluminum and yttrium to the selected cobalt alloy.
- the chart also shows the results of similar tests applied to samples of the nickel-base alloy Inconel 713C. It is obvious from the chart that the modified cobalt-base alloy X is far superior from a sulfidation resisting standpoint than the nickel-base alloy tested and it is far better than the unmodified cobalt-base alloy.
- Example III An accelerated oxidation-sulfidation test procedure was worked out and applied to the cobalt-base alloy WI-52, other cobalt-base alloys available on the market, and certain modified cobalt-base alloys including the one (alloy X) forming the subject matter of the present invention.
- the nominal chemical compositions of the alloys tested are shown in the chart illustrated in FIG. 3.
- the furnace in which the test was to be conducted was purged for thirty minutes with 2.0 c.f.h. N 0.072 c.f.h. C0 and 0.013 c.f.h. H 8.
- the test specimens were then placed in a silica retort which was in turn placed in the furnace and supplied with a gaseous mixture of 2.0 c.f.h. N 0.072 c.f.h. CO and 0.013 c.f.h. H 8 for two hours.
- the retort was supplied with a mixture of 2.0 c.f.h. air, 0.072 c.f.h. CO and 0.013 c.f.h.
- Example IV The sulfidation test procedure set forth in Example III was repeated with the exception that about 1 p.p.m. NaCl was introduced into the gas stream which contacted the alloy. This was accomplished by bubbling the synthetic gas combustion mixtures through a 10% salt solution. The comparative weight losses for the different alloys tested are set forth and graphically illustrated in FIG. 6.
- Example IV The sulfidation test procedure set forth in Example IV was repeated. Various alloys were tested with the results total amount of metals of the group is between about 3% and about 20% by weight of the total composition.
- composition of claim 5 wherein the respective individual amounts of tungsten and tantalum are between and compositions set forth in the following table: 5 about 4% and 10%, the amount of molybdenum is up to Composition, percent Sulfidation, Alloy wt. loss,
- cobalt-base alloys containing aluminum and yttrium possess vastly superior sulfidation resistance over other alloys including nickel-base alloys containing both aluminum and yttrium.
- the alloys of the invention may :also contain small amounts of phosphorus and sulfur and preferably in amounts not over 0.04%, silicon in an amount not over about 0.5%.
- Nickel may be present in amounts up to about 10% as well as iron and manganese in amounts up to about 2.5% in addition to small amounts of zirconium and boron.
- the absence or presence of these elements is not critical or necessary to the alloys of the invention.
- the superior sulfidation resistant cobalt-base alloys as disclosed herein may be used for a number of varied purposes.
- the alloy may be cast, rolled into sheets or prepared as bars or tubing for any uses where superior resistance to sulfur attack as well as oxidation is necessary.
- a sulfi'dation and oxidation resistant cobalt-base alloy comprising a major amount of cobalt and a small effective amount of the metals aluminum and yttrium in combination, the amount of aluminum and yttrium being effective to increase the sulfidation and oxidation resistance of the cobalt-base alloy.
- composition of claim 1 wherein the amount of aluminum is up to about 6.0% by weight and the amount of yttrium is up to about 3.0% by weight.
- composition of claim 1 wherein the amount of aluminum is at least about 1.0% by 'weight and the amount of yttrium is at least about 0.05% by weight.
- composition of claim 1 wherein the amount of aluminum is between about 1.0% and 6.0% by weight andthe amount of yttrium is between about 0.05 and 3.0% by weight.
- composition of claim 1 which contains one or more metals selected from the group consisting of tungsten, tantalum, molybdenum and columbium wherein the about 10% and the amount of columbium is up to about 2%.
- composition of claim 1 which contains up to about 25% chromium and between about 0.05% and about 0.5% by weight, carbon.
- a sulfidation and oxidation resistant cobalt-base alloy comprising cobalt, between about 1.0% and 6.0% aluminum, between about 0.05% and 3.0% yttrium, a total amount of between about 8% and 20% of one or more of the metals selected from the group consisting of tungsten, tantalum, molybdenum and columbium, between about 10% and 25% chromium and between about 0.05% and 0.5% carbon, with cobalt being the major metal present and wherein the percents specified are by weight of the total composition.
- composition of claim 8 wherein the amount of cobalt is between about 50% and about and wherein the mole ratios of aluminum and yttrium combined to cobalt is between 1:50 and 1:7, chromium to cobalt is between 1:5 and 2:5 and tungsten, tantalum and molybdenum and columbium combined to cobalt is between 1:6 and 1:3.
- composition of claim 9 which contains up to the following specified amounts of the following elements: 0.04% phosphorus, 0.04% sulfur, 0.5% silicon, 2.5% iron, 2.5% manganese, 10% nickel, 0.5% boron and 1.0% zirconium.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
Description
M. S. ROUSH Aug. 27, 1968 SULFIDATION AND OXIDATION RESISTANT COBALT-BASE ALLOY 4 Sheets-Sheet 2 Filed Jan. 25, 1967 Aug. 27, 1968 M. s. ROUSH 3,399,058
SULFIDATION AND OXIDATION RESISTANT COBALT-BASE ALLOY Filed Jan. 25, 1967 4 Sheets-Sheet 4.
2000 (I) O .J
I600 I700 000 I900 2000 TEMPERATURE, F
WEIGHT LOSS MG/SQJN. ALLOY |700F I800F I900F 2000F 0 INCONEL 7:30 400 1252 4200 owl-52 650 I220 3800 VWl-52+3%AL 2l5 410 720 I050 v Wl-52+|/2%Y 200 560 990 |5|5 o Wl-52+3%AL+I/2%Y(ALLOY-Z) 20 I9 3| 35 O ALLOY Z MODIFIED WITH Ni REPLACING ALL OF Co 600 I 810 43 5O SEVERE SULFIDATION TEST INVENTOR MILTON S. ROUSH ATTOR NEYS United States Patent 3,399,058 SULFIDATION AND OXIDATION RESISTANT COBALT-BASE ALLOY Milton S. Ronsh, Phoenix, Ariz., assignor to The Garrett Corporation, a corporation of California Continuation-impart of application Ser. No. 322,096, Nov. 7, 1963. This application Jan. 25, 1967, Ser. No. 617,755
Claims. (Cl. 75170) ABSTRACT OF THE DISCLOSURE A sulfidation and oxidation resistant cobalt-base alloy comprised of a major amount of cobalt, between about 0.05% and 3.0% by weight yttrium, between about 1.0% and 6.0% by weight aluminum and preferably also containing chromium, tungsten and/ or molybdenum, columbium and/ or tantalum and carbon.
This application is a continuation-in-part of my copending application Ser. No. 322,096, filed Nov. 7, 1963, now abandoned.
This invention relates generally to metal alloys and more particularly to alloys provided for use in the manufacture of machine parts, such as gas turbine wheels and/or blades, and nozzle vanes, which are exposed to high-temperature combustion gases containing oxygen, sulfur, lead, and/ or other chemicals that cause oxidation, sulfidation, corrosion and other deleterious effects.
Sulfidation is a metal deterioration which takes place particularly in the heated sections of gas turbines which are exposed to gaseous combustion products of sulfur and/ or lead containing fuels such as fuel oil, diesel fuel, aviation gasoline and the like. The problem is especially serious under desert or salt water atmosphere conditions where the presence of alkali or alkaline-earth metal salts such as sodium chloride, even in concentrations as low as 0.1 part per million, are found to catalyze the sulfidation reaction.
Heretofore, high-temperature metallurgy for use in oxygen containing environments has been limited to: (1) nickel-base alloys which, although oxidation resistant to 2000 F. are not satisfactory in sulfur containing atmospheres over 1650 especially when alkali and alkalineearth metal salts are present, or over 1750 F. when lead deposits are present; and (2) cobalt-base alloys which are resistant to sulfidation and lead attack up to 1850 F. but are not resistant to oxidation above 1750 F. These limitations seriously hamper the development of engines designed to operate with the presently available fuels which burn at 2000 F. or higher temperatures and contain lead, sulfur and other harmful gas-producing matter.
One aim of this invention is to provide an alloy having an equal or better oxidation resisting quality than the high strength nickel-base alloys, such as the alloy known as Inconel 713C, and an equal or better sulfidation resisting quality than the cobalt-base alloys, such as that identified by the trademark WI52.
In research performed prior to the conception of this invention, it was found that small amounts of rare earth metals, as well as yttrium, have been added to cobalt-base and iron-base alloys and as a result the amount of hightemperature oxidation of the alloys was reduced; the
ice
resistance, but once again the alloys are not resistant to sulfidation.
An object of this invention is to provide an alloy having high resistance to oxidation, sulfidation and lead corrosion when exposed, in oxygen containing environments, to gaseous products of combustion at about 2000 F. temperatures, such as are produced by burning JP4 or other gas turbine fuels.
It has been discovered that the resistance to oxidation, sulfidation and lead corrosion of cobalt-base alloys can be greatly increased by the addition of small percentages of aluminum and yttrium. Y
It is therefore another object of this invention to provide a cobalt-base alloy having at least about 1.0 weight percent aluminum and at least about 0.05 weight percent yttrium to increase the resistance of the alloy to oxidation, sulfidation and lead corrosion when exposed in air to gases resulting from the combustion of JP4 and/or other gas turbine fuels.
Still another object of the invention is to provide a cobalt-base alloy having a maximum of about 6.0 weight percent aluminum and a maximum of about 3.0 weight percent yttrium to further increase the resistance of the alloy to oxidation, sulfidation and lead corrosion when exposed to an atmosphere containing combustion products of fuels of the type employed to operate gas turbine engines.
The superior alloys of this invention are cobalt-base alloys containing a small amount of yttrium and aluminum and preferably a number of other metals which will improve the strength properties of the material. By the term cobalt-base alloy as used herein and as understood in the art, is meant a metallic composition wherein the major element present in cobalt and preferably wherein the cobalt is present in a major amount. More specifically it has been found according to the invention cobalt-base alloys containing from about 0.05 to about 3.0% by weight yttrium and from about 1.0 to about 6.0% by weight aluminum possess outstanding sulfidation and oxidation deterioration resistance.
Preferably the cobalt-base alloys of the invention contain between about 50% and 65% cobalt. In order to provide high strength cobalt-base alloys it is also necessary for the composition to contain tungsten and/or tantalum wherein the total amount of this group of metals is between about 3% and 20% by weight of the alloy composition. The preferred amounts of these metals individually are between 0% and 15% and more preferably between about 4% and 10% individually for tungsten and tantalum with the total amount of this group of metals being no more than about 20% by weight of the alloy composition. Alternatively, molybdenum may be present to replace all or part of the tungsten and columbium may be present to replace a part or all of the tantalum. Molybdenum preferably may be present up to about 10% and columbium up to about 2.0% by weight of the alloy composition. It is also desirable to have chromium present in order to provide a higher strength alloy for many uses. Thus, amounts of chromium up to about 25% and preferably between about 10% and about 25% may be used. The presence of a small amount of carbon also increases the strength of the alloy. However, where the carbon content gets above about 0.5% by Weight oxidation corrosion resistance may be sacrificed somewhat. Thus, suitable carbon concentrations are between about 0.05% and about 0.5% by Weight.
A convenient way to express the concentrations of the preferred cobalt-base alloys of this invention is by mole ratios based on cobalt. Thus, the preferred alloy composi- Patented Aug. 27, 1968 .tions corresponding to the concentrations as set forth above are as follows:
The yttrium used in the alloys of the invention may be pure or may be added as a yttrium composition referred to as a misch metal containing at least about 70% yttrium and a small amount of other elements such as lanthanum, cerium, neodymium, Samarium, gadolinium, dysprosium, erbium, ytterbium, etc., as Well as copper, calcium, magnesium, silicon and the like. When the yttrium is added to the alloy metal it is preferred to use vacuum conditions or those in which oxygen is absent in order to avoid large losses of yttrium due to oxidation.
The following examples are provided to illustrate the manner in which the invention is carried out. Unless otherwise indicated, parts and percents set forth are by weight.
Example I In carrying out the present invention, one of the presently available cobalt alloys, identified as WI-52 and having the following analysis:
Percent C 0.45 Cb+Ta 2.0
Percent Ni 74.2
Ob 2.0 Ti 0.8 A1 6.1
A graph is shown in FIG. 1 having curves to indicate the results of the tests. As shown in the upper left-hand corner of FIG. 1, the following symbols are used to identify the alloys and the curves plotted to illustrate the effect of the test thereon. It will be apparent from the graph that the cobalt alloy WI-SZ, modified to include small portions of both yttrium and aluminum, gained less weight and was therefore more oxidation resistant than the unmodified cobalt-base alloy or the alloy modified by the addition of either of the elements alone. The graph also shows that the alloy WI52 modified by the addition of 1% yttrium and 3% aluminum (designated X) 'has oxidation resisting qualities equal to the nickel-base alloy.
Example II Test samples of the modified cobalt-base alloy X were subjected to sulfidation resistance tests which. were run in an environment consisting of the combustion products of JP4 fuel (CO N 0 H O, S0 at elevated temperatures. After completion of the test the samples are cleaned by boiling in concentrated HNO and wire brushed. The cleaned samples are then weighed to determined any weight change. The results of such tests were compared with the results of similar tests made on the alloy WI-52 without modification and with the addition of a small part of yttrium alone. A chart, identified as FIG. 2 in the drawings, shows the increased resistance to sulfidation secured by the addition of similar small percentages of aluminum and yttrium to the selected cobalt alloy. The chart also shows the results of similar tests applied to samples of the nickel-base alloy Inconel 713C. It is obvious from the chart that the modified cobalt-base alloy X is far superior from a sulfidation resisting standpoint than the nickel-base alloy tested and it is far better than the unmodified cobalt-base alloy.
Example III An accelerated oxidation-sulfidation test procedure was worked out and applied to the cobalt-base alloy WI-52, other cobalt-base alloys available on the market, and certain modified cobalt-base alloys including the one (alloy X) forming the subject matter of the present invention. The nominal chemical compositions of the alloys tested are shown in the chart illustrated in FIG. 3.
The accelerated test procedure was as follows:
The furnace in which the test was to be conducted was purged for thirty minutes with 2.0 c.f.h. N 0.072 c.f.h. C0 and 0.013 c.f.h. H 8. The test specimens were then placed in a silica retort which was in turn placed in the furnace and supplied with a gaseous mixture of 2.0 c.f.h. N 0.072 c.f.h. CO and 0.013 c.f.h. H 8 for two hours. For the following twenty hours the retort was supplied with a mixture of 2.0 c.f.h. air, 0.072 c.f.h. CO and 0.013 c.f.h. S0 Specimens were cleaned and weighed following exposure to temperatures of 17 00 F, 1800 F., and 1900 F. for the twenty-two-hour period. The use of the two cycles during each test closely duplicates a gas turbine start when excess H S is present in the initial combustion products and continuous operation when S0 is found in the gaseous combustion products mixture. The weight losses for the different alloys are shown in the chart illustrated in FIG.-4. These weight-losses are graphically illustrated in FIG. 5 wherein the symbols used to identify the curves and alloys are shown in the upper left-hand corner. It is obvious from this graph that far better sulfidation resistance is secured with the alloy X forming the subject matter of the invention than with any other alloy tested. The graph shows that the addition of small parts of yttrium and aluminum improves the sulfidation resistance of the alloy HS-25, but alloy X is still better. Although this procedure subjected the specimens to more rigorous treatment than the parts of a turbine will normally be subjected to in actual use, the tenst definitely prove the superiority of the newly developed a 0 Example IV The sulfidation test procedure set forth in Example III was repeated with the exception that about 1 p.p.m. NaCl was introduced into the gas stream which contacted the alloy. This was accomplished by bubbling the synthetic gas combustion mixtures through a 10% salt solution. The comparative weight losses for the different alloys tested are set forth and graphically illustrated in FIG. 6.
The sulfidation test procedure set forth in Example IV was repeated. Various alloys were tested with the results total amount of metals of the group is between about 3% and about 20% by weight of the total composition.
6. The composition of claim 5 wherein the respective individual amounts of tungsten and tantalum are between and compositions set forth in the following table: 5 about 4% and 10%, the amount of molybdenum is up to Composition, percent Sulfidation, Alloy wt. loss,
C Cr Ta W Al Y Zr Mn Ni Fe mg./sq. in.,
73. 7 0. 10 20. 0 3.0 0. 45 0. 2. 24 3, 218 62.0 0. 48 20.9 11. 0 3. 1 .1 1 1, 200 73.8 0.10 20. 0 3. 0 1.4 0.40 0.5 0.83 104 70.5 0.10 20. 0 3.0 5.2 0.32 0.5 0.40 13 51. s 0.12 20. 0 9.8 2.4 0.10 0. 5 1.8 46 59.8 0. 11 20.0 14. 9 2. 73 0. 12 0. 5 1.8 80 57. 3 0. 12 20. 0 14. 0 5. 05 0. 0. 5 1. 9 18 69.8 0. 18. 1 3. 7 0. 9 0. 09 0. 19 0. 04 1, 090 69. 4 0. 11 17. 7 3. 7 2. 0 0. 14 0. 24 0. 04 110 03. 6 0.10 17. 6 3.8 2. 9 0.12 0.25 0.04 12 63.2 0. 23 14. 77 10. S8 3. 71 0. 09 0. 11 0. 01 05 50.1 .43 21. 4 15.1 3.2 0.6 0. 22 0. 10 57.8 .43 18.6 11.1 3.1 0. 5 0.19 0. 04 05 0. 19 20. 2 5. 4 3. 5 0. 12 0. 1s 0. 11 4, 270
1 Also contained B (0.004%). 2 Also contained 13 (0.18%).
As is evident from the results of the above-described sulfidation tests, those cobalt-base alloys containing aluminum and yttrium possess vastly superior sulfidation resistance over other alloys including nickel-base alloys containing both aluminum and yttrium. The alloys of the invention may :also contain small amounts of phosphorus and sulfur and preferably in amounts not over 0.04%, silicon in an amount not over about 0.5%. Nickel may be present in amounts up to about 10% as well as iron and manganese in amounts up to about 2.5% in addition to small amounts of zirconium and boron. However, the absence or presence of these elements is not critical or necessary to the alloys of the invention.
The superior sulfidation resistant cobalt-base alloys as disclosed herein may be used for a number of varied purposes. The alloy may be cast, rolled into sheets or prepared as bars or tubing for any uses where superior resistance to sulfur attack as well as oxidation is necessary.
What is claimed is:
1. A sulfi'dation and oxidation resistant cobalt-base alloy comprising a major amount of cobalt and a small effective amount of the metals aluminum and yttrium in combination, the amount of aluminum and yttrium being effective to increase the sulfidation and oxidation resistance of the cobalt-base alloy.
2. The composition of claim 1 wherein the amount of aluminum is up to about 6.0% by weight and the amount of yttrium is up to about 3.0% by weight.
3. The composition of claim 1 wherein the amount of aluminum is at least about 1.0% by 'weight and the amount of yttrium is at least about 0.05% by weight.
4. The composition of claim 1 wherein the amount of aluminum is between about 1.0% and 6.0% by weight andthe amount of yttrium is between about 0.05 and 3.0% by weight.
5. The composition of claim 1 which contains one or more metals selected from the group consisting of tungsten, tantalum, molybdenum and columbium wherein the about 10% and the amount of columbium is up to about 2%.
7. The composition of claim 1 which contains up to about 25% chromium and between about 0.05% and about 0.5% by weight, carbon.
8. A sulfidation and oxidation resistant cobalt-base alloy comprising cobalt, between about 1.0% and 6.0% aluminum, between about 0.05% and 3.0% yttrium, a total amount of between about 8% and 20% of one or more of the metals selected from the group consisting of tungsten, tantalum, molybdenum and columbium, between about 10% and 25% chromium and between about 0.05% and 0.5% carbon, with cobalt being the major metal present and wherein the percents specified are by weight of the total composition.
9. The composition of claim 8 wherein the amount of cobalt is between about 50% and about and wherein the mole ratios of aluminum and yttrium combined to cobalt is between 1:50 and 1:7, chromium to cobalt is between 1:5 and 2:5 and tungsten, tantalum and molybdenum and columbium combined to cobalt is between 1:6 and 1:3.
10. The composition of claim 9 which contains up to the following specified amounts of the following elements: 0.04% phosphorus, 0.04% sulfur, 0.5% silicon, 2.5% iron, 2.5% manganese, 10% nickel, 0.5% boron and 1.0% zirconium.
References Cited UNITED STATES PATENTS 2,304,353 12/1942 Grifiiths et a1 -171 2,513,471 7/1950 Franks et al. 75171 2,513,472 7/1950 Franks et al. 75171 2,703,355 3/1955 Hagglund 75171 2,920,956 1/1960 Nisbet et al. 75171 2,983,602 5/1961 Levinson et al. 75170 2,977,223 3/1961 BrOWn 75171 3,202,506 8/1965 Deutsch 75--171 RICHARD O. DEAN, Primary Examiner.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US617755A US3399058A (en) | 1963-11-07 | 1967-01-25 | Sulfidation and oxidation resistant cobalt-base alloy |
| GB0673/68A GB1210561A (en) | 1963-11-07 | 1968-01-11 | Oxidation, sulphidation and lead corrosion resistant alloy |
| DE19681608156 DE1608156A1 (en) | 1963-11-07 | 1968-01-19 | Metal alloy based on cobalt |
| FR137412A FR93750E (en) | 1963-11-07 | 1968-01-25 | Alloy resistant to corrosion by oxidation, sulfurization and the action of lead. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32209663A | 1963-11-07 | 1963-11-07 | |
| US617755A US3399058A (en) | 1963-11-07 | 1967-01-25 | Sulfidation and oxidation resistant cobalt-base alloy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3399058A true US3399058A (en) | 1968-08-27 |
Family
ID=24474927
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US617755A Expired - Lifetime US3399058A (en) | 1963-11-07 | 1967-01-25 | Sulfidation and oxidation resistant cobalt-base alloy |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3399058A (en) |
| DE (1) | DE1608156A1 (en) |
| FR (1) | FR93750E (en) |
| GB (1) | GB1210561A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3549354A (en) * | 1968-05-29 | 1970-12-22 | Garrett Corp | Sulfidation resistant cobalt-base alloys |
| US3907552A (en) * | 1971-10-12 | 1975-09-23 | Teledyne Inc | Nickel base alloys of improved properties |
| US3918139A (en) * | 1974-07-10 | 1975-11-11 | United Technologies Corp | MCrAlY type coating alloy |
| DE2655617A1 (en) * | 1975-12-08 | 1977-06-23 | United Technologies Corp | OXYDATION-RESISTANT COBALT-BASED ALLOY |
| US4088606A (en) * | 1974-05-06 | 1978-05-09 | Gould Inc. | Cobalt base nox reducing catalytic structure |
| US4459263A (en) * | 1982-09-08 | 1984-07-10 | Jeneric Industries, Inc. | Cobalt-chromium dental alloys containing ruthenium and aluminum |
| US4530664A (en) * | 1980-09-29 | 1985-07-23 | Jeneric Industries, Inc. | Cobalt-chromium alloys |
| US4606887A (en) * | 1983-05-28 | 1986-08-19 | Degussa Aktiengesellschaft | Cobalt alloys for the production of dental prothesis |
| US4837389A (en) * | 1984-06-04 | 1989-06-06 | Turbine Components Corporation | Composite alloy structures |
| US6756012B2 (en) | 2000-08-10 | 2004-06-29 | Jeneric/Pentron, Inc. | High expansion dental alloys |
| EP1925683A4 (en) * | 2005-09-15 | 2012-08-22 | Japan Science & Tech Agency | COBALT BASED ALLOY WITH HIGH HEAT RESISTANCE AND HIGH STRENGTH AND MANUFACTURING METHOD THEREFOR |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2304353A (en) * | 1935-05-09 | 1942-12-08 | Int Nickel Co | Heat resistant alloy |
| US2513472A (en) * | 1946-05-09 | 1950-07-04 | Union Carbide & Carbon Corp | Alloy articles for use at high temperatures |
| US2513471A (en) * | 1946-05-09 | 1950-07-04 | Union Carbide & Carbon Corp | Alloy articles for high-temperature service |
| US2703355A (en) * | 1950-10-23 | 1955-03-01 | Kanthal Corp | Electric heater |
| US2920956A (en) * | 1956-10-08 | 1960-01-12 | Universal Cyclops Steel Corp | Method of preparing high temperature alloys |
| US2977223A (en) * | 1957-12-10 | 1961-03-28 | Westinghouse Electric Corp | Stabilized and precipitation-hardened nickel-base alloys |
| US2983602A (en) * | 1957-09-24 | 1961-05-09 | Armour Res Found | Cobalt alloys |
| US3202506A (en) * | 1963-01-23 | 1965-08-24 | David E Deutsch | High-temperature oxidation-resistant cobalt base alloys |
-
1967
- 1967-01-25 US US617755A patent/US3399058A/en not_active Expired - Lifetime
-
1968
- 1968-01-11 GB GB0673/68A patent/GB1210561A/en not_active Expired
- 1968-01-19 DE DE19681608156 patent/DE1608156A1/en active Pending
- 1968-01-25 FR FR137412A patent/FR93750E/en not_active Expired
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2304353A (en) * | 1935-05-09 | 1942-12-08 | Int Nickel Co | Heat resistant alloy |
| US2513472A (en) * | 1946-05-09 | 1950-07-04 | Union Carbide & Carbon Corp | Alloy articles for use at high temperatures |
| US2513471A (en) * | 1946-05-09 | 1950-07-04 | Union Carbide & Carbon Corp | Alloy articles for high-temperature service |
| US2703355A (en) * | 1950-10-23 | 1955-03-01 | Kanthal Corp | Electric heater |
| US2920956A (en) * | 1956-10-08 | 1960-01-12 | Universal Cyclops Steel Corp | Method of preparing high temperature alloys |
| US2983602A (en) * | 1957-09-24 | 1961-05-09 | Armour Res Found | Cobalt alloys |
| US2977223A (en) * | 1957-12-10 | 1961-03-28 | Westinghouse Electric Corp | Stabilized and precipitation-hardened nickel-base alloys |
| US3202506A (en) * | 1963-01-23 | 1965-08-24 | David E Deutsch | High-temperature oxidation-resistant cobalt base alloys |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3549354A (en) * | 1968-05-29 | 1970-12-22 | Garrett Corp | Sulfidation resistant cobalt-base alloys |
| US3907552A (en) * | 1971-10-12 | 1975-09-23 | Teledyne Inc | Nickel base alloys of improved properties |
| US4088606A (en) * | 1974-05-06 | 1978-05-09 | Gould Inc. | Cobalt base nox reducing catalytic structure |
| US3918139A (en) * | 1974-07-10 | 1975-11-11 | United Technologies Corp | MCrAlY type coating alloy |
| DE2655617A1 (en) * | 1975-12-08 | 1977-06-23 | United Technologies Corp | OXYDATION-RESISTANT COBALT-BASED ALLOY |
| US4078922A (en) * | 1975-12-08 | 1978-03-14 | United Technologies Corporation | Oxidation resistant cobalt base alloy |
| US4530664A (en) * | 1980-09-29 | 1985-07-23 | Jeneric Industries, Inc. | Cobalt-chromium alloys |
| US4459263A (en) * | 1982-09-08 | 1984-07-10 | Jeneric Industries, Inc. | Cobalt-chromium dental alloys containing ruthenium and aluminum |
| US4606887A (en) * | 1983-05-28 | 1986-08-19 | Degussa Aktiengesellschaft | Cobalt alloys for the production of dental prothesis |
| US4837389A (en) * | 1984-06-04 | 1989-06-06 | Turbine Components Corporation | Composite alloy structures |
| US6756012B2 (en) | 2000-08-10 | 2004-06-29 | Jeneric/Pentron, Inc. | High expansion dental alloys |
| EP1925683A4 (en) * | 2005-09-15 | 2012-08-22 | Japan Science & Tech Agency | COBALT BASED ALLOY WITH HIGH HEAT RESISTANCE AND HIGH STRENGTH AND MANUFACTURING METHOD THEREFOR |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1608156A1 (en) | 1970-12-03 |
| GB1210561A (en) | 1970-10-28 |
| FR93750E (en) | 1969-05-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Mankins et al. | Nickel and nickel alloys | |
| US4261742A (en) | Platinum group metal-containing alloys | |
| US3399058A (en) | Sulfidation and oxidation resistant cobalt-base alloy | |
| CA1090168A (en) | Oxidation resistant cobalt base alloy | |
| JPH086164B2 (en) | Method for enhancing crevice and pitting corrosion resistance of nickel-base alloys | |
| US3516826A (en) | Nickel-chromium alloys | |
| GB2033925A (en) | Nickel based superalloys | |
| US3723108A (en) | Nickel-chromium-cobalt alloys | |
| US3589894A (en) | Sulfidation resistant cobalt-base alloy | |
| US2948606A (en) | High temperature nickel base alloy | |
| CN108330336A (en) | A kind of high antioxygenic property group of the lanthanides nickel base superalloy and its preparation method and application | |
| US3549354A (en) | Sulfidation resistant cobalt-base alloys | |
| US3486885A (en) | Stainless steel alloy with low phosphorus content | |
| US2536034A (en) | High-temperature stainless steel | |
| US2764481A (en) | Iron base austenitic alloys | |
| US3849189A (en) | Flux coated electrode | |
| US3925070A (en) | Brazing alloy | |
| JP2992226B2 (en) | Nickel alloys having corrosion resistance and construction members made from these alloys | |
| US3617263A (en) | Corrosion-resistant nickel-chromium base alloy | |
| US3202506A (en) | High-temperature oxidation-resistant cobalt base alloys | |
| JPS644579B2 (en) | ||
| Smith | Oxidation resistance of high‐alloy steels: Part 2 | |
| Heubner | Nickel alloys and high-alloy special stainless steels-materials summary and metallurgical principles | |
| US3346378A (en) | Cobalt base alloys | |
| US2661284A (en) | Precipitation hardenable iron base alloy |