US3078554A - Columbium base alloy article - Google Patents
Columbium base alloy article Download PDFInfo
- Publication number
- US3078554A US3078554A US34632A US3463260A US3078554A US 3078554 A US3078554 A US 3078554A US 34632 A US34632 A US 34632A US 3463260 A US3463260 A US 3463260A US 3078554 A US3078554 A US 3078554A
- Authority
- US
- United States
- Prior art keywords
- aluminum
- alloy
- columbium
- alloys
- weight
- 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 claims description 57
- 239000000956 alloy Substances 0.000 title claims description 57
- 239000010955 niobium Substances 0.000 title claims description 33
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 title claims description 31
- 230000003647 oxidation Effects 0.000 claims description 31
- 238000007254 oxidation reaction Methods 0.000 claims description 31
- 229910052782 aluminium Inorganic materials 0.000 claims description 26
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 26
- 238000000576 coating method Methods 0.000 claims description 24
- 239000011248 coating agent Substances 0.000 claims description 21
- 239000010936 titanium Substances 0.000 description 27
- 229910052719 titanium Inorganic materials 0.000 description 25
- 229910000838 Al alloy Inorganic materials 0.000 description 18
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 18
- 229910052710 silicon Inorganic materials 0.000 description 10
- 238000007598 dipping method Methods 0.000 description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- 238000007792 addition Methods 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 238000005422 blasting Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 239000012080 ambient air Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229910052790 beryllium Inorganic materials 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000003870 refractory metal Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 241000220010 Rhode Species 0.000 description 1
- 229910002796 Si–Al Inorganic materials 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
- C23C10/18—Solid state diffusion of only metal elements or silicon into metallic material surfaces using liquids, e.g. salt baths, liquid suspensions
- C23C10/20—Solid state diffusion of only metal elements or silicon into metallic material surfaces using liquids, e.g. salt baths, liquid suspensions only one element being diffused
- C23C10/22—Metal melt containing the element to be diffused
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/934—Electrical process
- Y10S428/935—Electroplating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/937—Sprayed metal
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/938—Vapor deposition or gas diffusion
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/939—Molten or fused coating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/12743—Next to refractory [Group IVB, VB, or VIB] metal-base component
Definitions
- One method of increasing oxidation resistance is to diffuse into the surface of columbium base alloys certain alloying elements, such as aluminum, so that through the subsequent formation of stable compounds, oxidation resistance is imparted to the alloy.
- Coatings of aluminum have been known to increase the oxidation resistance of iron, copper, cobalt and nickel base alloys.
- Application methods include dipping into molten aluminum or aluminum alloy baths, spraying on molten aluminum, flame depositing semimolten aluminum or its alloys, vapor deposition and the like.
- Aluminum alloys suitable for use as coating materials have been reported to include small additions of Be, Ce, Cr, Cu, Co, Mg, Mo, Si, Ti, V and Zn all of which are said to impart increased oxidation resistance to the coated article.
- a principal object of this invention is to provide a columbium base alloy article of improved oxidation resistance, imparted thereto through a unique aluminum base alloy coating.
- the present invention provides an improved oxidation resistant columbium base alloy article including between ll% titanium and coated with an aluminum base alloy comprising 5l5% by weight silicon with the balance aluminum.
- this invention provides an improved oxidation resistant columbium base alloy article coated with an aluminum base alloy comprising ll0% by weight titanium, 5-15 by Weight silicon with the balance aluminum.
- the preferred method by which the article of this invention is made is through the use of a molten aluminum alloy bath into which the article can be dipped, although it is contemplated that such aluminum alloy coating can be applied by the many deposition processes well known in the art. These include but are not limited to spraying of molten metal, spraying of powder coupled with further heat treatment, vapor deposition, electrodeposition followed by heat treatment, etc.
- Molten aluminum and molten aluminum alloy baths are well known as a method of imparting oxidation resistance to various materials.
- the inclusion of silicon within the range of 5-15 by weight similarly are well known in this art.
- additions to such Si-Al alloys such as Be, Ce, Cr, Cu, Co, Mg, Mo, Si, Ti, V and Zn do not always result in improved oxidation resistance when applied to columbium base alloys, and have been shown not to be equivalents.
- the samples were then dipped in a 15 Si, balance Al alloy which had been pre-alloyed in an argon atmosphere induction furnace and re-melted in a graphite crucible under a nitrogen blanket.
- the remelted aluminum alloy was covered with a standard commercial fluoride-containing brazing flux (Alcoa #30).
- Alcoa #30 a standard commercial fluoride-containing brazing flux
- the samples were dipped from one to thirteen minutes at a temperature of 1500-1900 F. after which they were removed from the molten aluminum and excess aluminum was removed by vigorously shaking the samples. After the dipping operation, the samples were heat treated at 1700-2100 F. for one hour in argon.
- the samples were then oxidized in static, ambient air for twenty-four hours at 2300 F.
- the optimum post-treatment was for one hour at about 1900 F. in vacuum.
- the specimens were mounted on a piece of molybdenum mesh and supported by tantalum wire.
- a vacuum of 0.02 micron was obtained in the furnace in which the samples were treated.
- the samples were removed from the heated portion of the furnace and allowed to cool in vacuum, in this case for one hour, before opening to the atmosphere. 7
- columbium alloy D including 8% by weight titanium and coated with aluminum coating alloy 1 including no titanium, an improved oxid tion resistance is obtained over columbium base alloys not including titanium although the addition of small amounts of titanium up to about l0% by weight improves the oxidation resistance of such alloys.
- columbium alloy A which had been dipped into a molten bath of aluminum 2 without prior vapor blasting of the surface of the sample resulted in a weight gain after two hours of 8.6, after four hours of 12.6 and after twenty-four hours of 84.7 all of which are significantly greater than the vapor blasted sample of Table III.
- a columbium base alloy article of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 5-15 Si, 1l0% Ti with the balance aluminum.
- a columbium base alloy article of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 5-15 Si, l-5% Ti with the balance aluminum.
- a columbium base alloy article of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 515% Si, about 5% Ti with the balance aluminum.
- a columbium base alloy article including from a small amount up to about 10% by weight titanium of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 515% Si, 110% Ti with the balance aluminum.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Coating With Molten Metal (AREA)
Description
United States Patent Ofitice 3,078,554 Patented Feb. 26, 1963 3,978,554 QQLUMTBTUM BASE ALLOY ARTICLE Robert G. Carlson, Greenhilis, Ohio, assignor to General Electric Company, a corporation of New York No Drawing. Filed .iune 8, 1960, Ser. No. 34,632 4- Claims. (Cl. 29-194) This invention relates to columbium base alloys and, more particularly, to an oxidation resistant coating for columbium base alloy articles.
As the technology in the art of power producing apparatus, such as gas turbines, advances and becomes more complex, there is an ever increasing need for materials which have high strength at the high temperature operating conditions of such complex apparatus coupled with resistance to oxidation. Alloys of the refractory metal columbium have a great potential for structural applica tions at elevated temperatures, not only because of their high strength-to-weight ratio, but also because of their relatively low rates of oxidation as compared with other fabricable refractory metals and alloys. However, even though the oxidation rates of columbium base alloys are comparatively low, they still oxidize at the rate of 2 to 3 times greater than acceptable values. Hence, surface protection of these alloys is mandatory for practical applications.
One method of increasing oxidation resistance is to diffuse into the surface of columbium base alloys certain alloying elements, such as aluminum, so that through the subsequent formation of stable compounds, oxidation resistance is imparted to the alloy.
Coatings of aluminum have been known to increase the oxidation resistance of iron, copper, cobalt and nickel base alloys. Application methods include dipping into molten aluminum or aluminum alloy baths, spraying on molten aluminum, flame depositing semimolten aluminum or its alloys, vapor deposition and the like.
Aluminum alloys suitable for use as coating materials have been reported to include small additions of Be, Ce, Cr, Cu, Co, Mg, Mo, Si, Ti, V and Zn all of which are said to impart increased oxidation resistance to the coated article.
A principal object of this invention is to provide a columbium base alloy article of improved oxidation resistance, imparted thereto through a unique aluminum base alloy coating.
This and other objects and advantages will become more apparent from the following detailed description which is meant to be exemplary rather than a limitation on the broad scope of the present invention.
It has been found that in order to impart improved oxidation resistance to a columbium base alloy article, the columbium base alloy itself, prior to manufacture into an article, should be first alloyed with between 1l0% by weight titanium. Therefore, in one form, the present invention provides an improved oxidation resistant columbium base alloy article including between ll% titanium and coated with an aluminum base alloy comprising 5l5% by weight silicon with the balance aluminum. In another form, this invention provides an improved oxidation resistant columbium base alloy article coated with an aluminum base alloy comprising ll0% by weight titanium, 5-15 by Weight silicon with the balance aluminum.
The preferred method by which the article of this invention is made is through the use of a molten aluminum alloy bath into which the article can be dipped, although it is contemplated that such aluminum alloy coating can be applied by the many deposition processes well known in the art. These include but are not limited to spraying of molten metal, spraying of powder coupled with further heat treatment, vapor deposition, electrodeposition followed by heat treatment, etc.
Molten aluminum and molten aluminum alloy baths are well known as a method of imparting oxidation resistance to various materials. The inclusion of silicon within the range of 5-15 by weight similarly are well known in this art. However, additions to such Si-Al alloys such as Be, Ce, Cr, Cu, Co, Mg, Mo, Si, Ti, V and Zn do not always result in improved oxidation resistance when applied to columbium base alloys, and have been shown not to be equivalents.
- It had been recognized that an aluminum base alloy including about 15% by weight silicon imparted the best oxidation resistance to a columbium base alloy including nominally about 10% by weight titanium. In order to determine and evaluate dipping and post-treatment parameters on the 2300 F. oxidation resistance of such a titanium bearing columbium alloy, 15 centerless ground 0.353" diameter by /2" long samples were ground from an arc melted columbium base alloy after extrusion and consisting essentially in percent by weight of 6.8% Ti, 6.35% Mo, 0.34% Zr, with the balance Cb. The surface of the sample was first activated by vapor blasting and was then washed with Water. The samples were then dipped in a 15 Si, balance Al alloy which had been pre-alloyed in an argon atmosphere induction furnace and re-melted in a graphite crucible under a nitrogen blanket. The remelted aluminum alloy was covered with a standard commercial fluoride-containing brazing flux (Alcoa #30). The samples were dipped from one to thirteen minutes at a temperature of 1500-1900 F. after which they were removed from the molten aluminum and excess aluminum was removed by vigorously shaking the samples. After the dipping operation, the samples were heat treated at 1700-2100 F. for one hour in argon. The samples were then oxidized in static, ambient air for twenty-four hours at 2300 F. The results of this testing indicated that an optimum dipping time and temperature and posttreatment was about three minutes at about 1700 F. and a post-treatment in vacuum for about one hour at about 1900* F. This same series of tests was repeated on samples of alloys A, B, C, and D of Table I below as well as on unalloyed columbium for one, two and three minutes. It was shown that an optimum oxidation resistance condition for a minimum coating thickness (10 mils) can be attained by a three minute dip at 1700 F. with a posttreatment in vacuum for one hour at about 1900 F., al-
though it was recognized that slightly greater oxidation resistance can be obtained by dipping for longer times and/or higher temperatures to obtain greater coating thicknesses.
In order to determine the effects of the number of variables on the oxidation resistance of columbium and cobium base alloys to which various aluminum base alloys were applied. 1
TABLE I Percent by weight Ob alloy V l W, Mo Ta. Zr Ti Cb'.'
0. f 0 Balance.
1 O Do. 1 5 Do.
Samples of the above listed columbium base alloys were used in the form of sheets about A" square. These samples were prepared in a manner the same as described above prior to the aluminum alloy dip. The samples were than dipped at 1700 F. for three minutes under an argon protective atmosphere in the aluminum alloys listed in Table II.
TABLE II Percent by weight A! alloy Si Ti Cu Mg The diificulty was encountered by the inability of the aluminum alloys containing magnesium to uniformly coat the samples; further study on the alloys containing magnesium was discontinued.
Immediately after withdrawing the dipped samples from the bath, the excess aluminum alloy was removed by vigorously shaking. Following the dipping operation the samples were post-treated at 1900 F. for one hour. All samples were initially weighed separately and then oxidized for twenty-four hours at 2300 F. in static, ambient air. The samples were removed from the furnace and weighed after two, four and twenty-four hours. The weight gain in mg./cm. vs. time of exposure at 2300 F. is given in the following Table III.
TABLE III Oxidation Test at 2300" F.
Weight; gain (mg/cm!) Cb alloy A1 alloy 2 hours 4 hours 24 hours A Ti) 2(10 Ti).- 5.5 7.9 13. 9
(5 Cul 96.5 4 011).- 38. 2 100. 8 13(0 Tl) 1 (0 Ti)--- 6.4 14.6 177.5 3 (5 'Ii) 4.9 7.0 11.1 2 (10 Ti)- 10.0 15. 2 22. 4 5 (5 Cu)-.- 47. 3 108. 9 267. 0 4 (10 011).. 48.6 169.0 C (5 Ti) 1 (0 Ti) 5. 5 12. 0 140. 1 3 (5 Ti)--- 4. 9 5. 7 7. 7 2 (10 Ti) 6.0 7. 8 23. 3 5 (5 Cu) 39. 5 54.4 175.8 4 (10 Cu 42. 5 93.8 222.5 D (8 Ti) 1 (0 Ti)--- 1.3 3.4 48.5 3 (5 Ii) 4.4 6.6 10.7 2 (l0 Ti) 4.9 15.1 36.2 5 (5 Cu).. 10. 7 35. 6 123.0 4 (10 011).- 11.0 35. 3
1 Completely oxidized.
As was mentioned above the optimum post-treatment was for one hour at about 1900 F. in vacuum. In the vacuum post-treatments, the specimens were mounted on a piece of molybdenum mesh and supported by tantalum wire. A vacuum of 0.02 micron was obtained in the furnace in which the samples were treated. At the completion of the testing the samples were removed from the heated portion of the furnace and allowed to cool in vacuum, in this case for one hour, before opening to the atmosphere. 7
Referring now to Table III above it can be easily seen that the inclusion of up to about 10% by weight titanium in the aluminum coating alloy or the inclusion of titanium in the columbium alloy alone or in combination with titanium in the aluminum coating alloy results in a system affording significantly improved oxidation resistance as compared with such alloys or such coatings not including titanium up to about 10% by Weight. It is readily observed that the copper bearing aluminum coating alloys were very detrimental. Referring to columbium alloy B in which no titanium is included, it can be observed in Table III that the addition of 5-l0% titanium in the coating alloy significantly improves the long time oxidation resistance although it is apparent from the comparison of aluminum alloy coating 3 with 2 when applied to columbium alloys B, C and D that an optimum value of titanium in the coating is in the range somewhat less than 10% by weight. Referring to columbium alloy D including 8% by weight titanium and coated with aluminum coating alloy 1 including no titanium, an improved oxid tion resistance is obtained over columbium base alloys not including titanium although the addition of small amounts of titanium up to about l0% by weight improves the oxidation resistance of such alloys.
Therefore, although aluminum alloy coatings for oxidation resistance which may include 5-15% by weight silicon and a number of other addition elements will impart an oxidation resistance to a number of varieties of alloys such as those based on iron, nickel, cobalt and the like, this has not been found to be necessarily true for columbium base alloys. This invention in one form recognizes that an unexpected improvement in oxidation resistance can be achieved by the addition of up to about 10% titanium in an aluminum coating bath including 515% silicon.
In addition to the optimum method for coating and treating columbium alloys as has been described above it has been found that activating the surface such as by vapor blasting prior to application of the aluminum alloy coating such as through dipping is very significant. For example referring to Table III above, columbium alloy A which had been dipped into a molten bath of aluminum 2 without prior vapor blasting of the surface of the sample resulted in a weight gain after two hours of 8.6, after four hours of 12.6 and after twenty-four hours of 84.7 all of which are significantly greater than the vapor blasted sample of Table III.
Although this invention has been described in connection with specific examples, these examples are meant to be illustrative of rather than limitations on the broad scope of the invention.
What is claimed is:
1. A columbium base alloy article of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 5-15 Si, 1l0% Ti with the balance aluminum.
2. A columbium base alloy article of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 5-15 Si, l-5% Ti with the balance aluminum.
3. A columbium base alloy article of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 515% Si, about 5% Ti with the balance aluminum.
4. A columbium base alloy article including from a small amount up to about 10% by weight titanium of improved oxidation resistance having a coating of an aluminum alloy consisting essentially of, in percent by weight, about 515% Si, 110% Ti with the balance aluminum.
References Cited in the file of this patent UNITED STATES PATENTS 1,121,169 Cooper Dec. 15, 1914 1,815,638 Watkins July 21, 1931 2,793,423 Stumbock May 28, 1957 2,824,359 Rhodes Feb. 25, 1958
Claims (1)
1. A COLUMBIUM BASE ALLOY ARTICLE OF IMPROVED OXIDATION RESISTANCE HAVING A COATING OF AN ALUMIUNM ALLOY CONSISTING ESSENTIALLY OF, IN PERCENT BY WEIGHT, ABOUT 5-15% SI, 1-10% TI WITH THE BALANCE ALUMINUM.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34632A US3078554A (en) | 1960-06-08 | 1960-06-08 | Columbium base alloy article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34632A US3078554A (en) | 1960-06-08 | 1960-06-08 | Columbium base alloy article |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3078554A true US3078554A (en) | 1963-02-26 |
Family
ID=21877623
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US34632A Expired - Lifetime US3078554A (en) | 1960-06-08 | 1960-06-08 | Columbium base alloy article |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3078554A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3181936A (en) * | 1960-12-30 | 1965-05-04 | Gen Electric | Superconductors and method for the preparation thereof |
| US3184292A (en) * | 1964-07-08 | 1965-05-18 | Du Pont | Process and composition for diffusion coating refractory metals and product produced thereby |
| US3186070A (en) * | 1961-07-03 | 1965-06-01 | Gen Electric | Protective coatings and process for producing the same |
| US3206289A (en) * | 1961-11-07 | 1965-09-14 | United Aircraft Corp | Coated columbium alloy articles |
| US3262764A (en) * | 1963-08-19 | 1966-07-26 | United Aircraft Corp | Coatings for columbium base alloys |
| US3268362A (en) * | 1961-05-26 | 1966-08-23 | Rca Corp | Deposition of crystalline niobium stannide |
| US3268306A (en) * | 1962-03-28 | 1966-08-23 | Trw Inc | Titanium pretreatment for protective coating of refractory alloys |
| US3300854A (en) * | 1964-05-14 | 1967-01-31 | Mcdonnell Aircraft | Method of making refractory metal structures with an oxidation resistant coating |
| US3342564A (en) * | 1965-01-22 | 1967-09-19 | Martin Metals Company | Composite castings |
| US3431141A (en) * | 1966-02-18 | 1969-03-04 | Kawecki Chem Co | High temperature oxidation resistant articles |
| US3489535A (en) * | 1966-10-03 | 1970-01-13 | United Aircraft Corp | Coatings for refractory-metalbase alloys |
| US3492102A (en) * | 1966-03-16 | 1970-01-27 | United Aircraft Corp | Refractory metal articles protected from atmospheric contamination at elevated temperatures by surface coatings |
| US3503791A (en) * | 1965-08-30 | 1970-03-31 | Electro Chimie Metal | Process of forming an alumino-silicide layer on a metal part |
| US3578743A (en) * | 1969-01-13 | 1971-05-18 | United Aircraft Corp | Aluminum coated columbium base alloys |
| US3710844A (en) * | 1967-02-24 | 1973-01-16 | Hitachi Ltd | Method of producing superconducting strips |
| US3765953A (en) * | 1970-08-12 | 1973-10-16 | Socinat Etude & De Constructio | Niobium-based oxidation resistant materials and process for their preparation |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1121169A (en) * | 1913-05-12 | 1914-12-15 | George Cooper | Process for coating a metallic body. |
| US1815638A (en) * | 1929-05-24 | 1931-07-21 | Copper Plate Sheet & Tube Comp | Process of plating metal |
| US2793423A (en) * | 1954-04-19 | 1957-05-28 | Baker & Co Inc | Compound metal stock |
| US2824359A (en) * | 1948-08-05 | 1958-02-25 | Int Nickel Co | Fabricated gas turbine structures |
-
1960
- 1960-06-08 US US34632A patent/US3078554A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1121169A (en) * | 1913-05-12 | 1914-12-15 | George Cooper | Process for coating a metallic body. |
| US1815638A (en) * | 1929-05-24 | 1931-07-21 | Copper Plate Sheet & Tube Comp | Process of plating metal |
| US2824359A (en) * | 1948-08-05 | 1958-02-25 | Int Nickel Co | Fabricated gas turbine structures |
| US2793423A (en) * | 1954-04-19 | 1957-05-28 | Baker & Co Inc | Compound metal stock |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3181936A (en) * | 1960-12-30 | 1965-05-04 | Gen Electric | Superconductors and method for the preparation thereof |
| US3268362A (en) * | 1961-05-26 | 1966-08-23 | Rca Corp | Deposition of crystalline niobium stannide |
| US3186070A (en) * | 1961-07-03 | 1965-06-01 | Gen Electric | Protective coatings and process for producing the same |
| US3206289A (en) * | 1961-11-07 | 1965-09-14 | United Aircraft Corp | Coated columbium alloy articles |
| US3268306A (en) * | 1962-03-28 | 1966-08-23 | Trw Inc | Titanium pretreatment for protective coating of refractory alloys |
| US3262764A (en) * | 1963-08-19 | 1966-07-26 | United Aircraft Corp | Coatings for columbium base alloys |
| US3300854A (en) * | 1964-05-14 | 1967-01-31 | Mcdonnell Aircraft | Method of making refractory metal structures with an oxidation resistant coating |
| US3184292A (en) * | 1964-07-08 | 1965-05-18 | Du Pont | Process and composition for diffusion coating refractory metals and product produced thereby |
| US3342564A (en) * | 1965-01-22 | 1967-09-19 | Martin Metals Company | Composite castings |
| US3503791A (en) * | 1965-08-30 | 1970-03-31 | Electro Chimie Metal | Process of forming an alumino-silicide layer on a metal part |
| US3431141A (en) * | 1966-02-18 | 1969-03-04 | Kawecki Chem Co | High temperature oxidation resistant articles |
| DE1646629B1 (en) * | 1966-02-18 | 1971-10-14 | Kawecki Chem Co | HIGHLY FIRE-RESISTANT OBJECT |
| US3492102A (en) * | 1966-03-16 | 1970-01-27 | United Aircraft Corp | Refractory metal articles protected from atmospheric contamination at elevated temperatures by surface coatings |
| US3489535A (en) * | 1966-10-03 | 1970-01-13 | United Aircraft Corp | Coatings for refractory-metalbase alloys |
| US3710844A (en) * | 1967-02-24 | 1973-01-16 | Hitachi Ltd | Method of producing superconducting strips |
| US3578743A (en) * | 1969-01-13 | 1971-05-18 | United Aircraft Corp | Aluminum coated columbium base alloys |
| US3765953A (en) * | 1970-08-12 | 1973-10-16 | Socinat Etude & De Constructio | Niobium-based oxidation resistant materials and process for their preparation |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3078554A (en) | Columbium base alloy article | |
| US3415672A (en) | Method of co-depositing titanium and aluminum on surfaces of nickel, iron and cobalt | |
| US4070507A (en) | Platinum-rhodium-containing high temperature alloy coating method | |
| US3951642A (en) | Metallic coating powder containing Al and Hf | |
| US2665475A (en) | Highly refractory body | |
| US3057048A (en) | Protection of niobium | |
| US4084025A (en) | Process of applying protective aluminum coatings for non-super-strength nickel-chromium alloys | |
| EP0510950A1 (en) | Treatment of sintered alloys | |
| US3996021A (en) | Metallic coated article with improved resistance to high temperature environmental conditions | |
| US3305384A (en) | Process for producing corrosion-resistant aluminum-coated iron surfaces | |
| US2924004A (en) | Refractory metal bodies | |
| US2988807A (en) | Method of aluminizing cobalt base alloys and article resulting therefrom | |
| GB1431517A (en) | Method of coating metallic substrates with aluminium alloys | |
| US2788289A (en) | Method of forming protective coatings for molybdenum and molybdenum-base alloys | |
| US4071638A (en) | Method of applying a metallic coating with improved resistance to high temperature to environmental conditions | |
| US3577268A (en) | Method of coating iron,nickel or cobalt alloy with aluminum | |
| US2752268A (en) | Process of making alluminum coated ferrous bodies | |
| US3639107A (en) | Hot-dip-aluminizing alloy | |
| JPH03229846A (en) | Galvanized material and galvanizing method | |
| US3184330A (en) | Diffusion process | |
| US3015579A (en) | Metal coating process | |
| US2782493A (en) | Aluminum coated ferrous article | |
| US3055771A (en) | Method of coating a ferrous base with aluminum | |
| US3342628A (en) | Alloy diffusion process | |
| US3019516A (en) | Method of forming a protective coating on molybdenum |