US2711975A - Vitreous coated refractory metals, method for producing the same, and vitreous enamel composition - Google Patents
Vitreous coated refractory metals, method for producing the same, and vitreous enamel composition Download PDFInfo
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- US2711975A US2711975A US102708A US10270849A US2711975A US 2711975 A US2711975 A US 2711975A US 102708 A US102708 A US 102708A US 10270849 A US10270849 A US 10270849A US 2711975 A US2711975 A US 2711975A
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- coating
- oxide
- vitreous
- glass
- metal
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- 239000000203 mixture Substances 0.000 title claims description 25
- 239000003870 refractory metal Substances 0.000 title description 15
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000000037 vitreous enamel Substances 0.000 title description 2
- 238000000576 coating method Methods 0.000 claims description 50
- 239000011248 coating agent Substances 0.000 claims description 43
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- 229910011255 B2O3 Inorganic materials 0.000 claims description 14
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 13
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 11
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 11
- 239000000292 calcium oxide Substances 0.000 claims description 9
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 9
- 238000005260 corrosion Methods 0.000 claims description 9
- 230000007797 corrosion Effects 0.000 claims description 9
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000011521 glass Substances 0.000 description 31
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 238000007792 addition Methods 0.000 description 14
- 229910052750 molybdenum Inorganic materials 0.000 description 14
- 239000011733 molybdenum Substances 0.000 description 14
- 239000002585 base Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000010304 firing Methods 0.000 description 8
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 235000012239 silicon dioxide Nutrition 0.000 description 7
- 239000010953 base metal Substances 0.000 description 6
- 150000001339 alkali metal compounds Chemical class 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229920000609 methyl cellulose Polymers 0.000 description 4
- 239000001923 methylcellulose Substances 0.000 description 4
- 235000010981 methylcellulose Nutrition 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910052752 metalloid Inorganic materials 0.000 description 3
- 150000002738 metalloids Chemical class 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- -1 aluminum silicates Chemical class 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 229910001634 calcium fluoride Inorganic materials 0.000 description 2
- 238000005524 ceramic coating Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229910001080 W alloy Inorganic materials 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- MGRWKWACZDFZJT-UHFFFAOYSA-N molybdenum tungsten Chemical compound [Mo].[W] MGRWKWACZDFZJT-UHFFFAOYSA-N 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
- C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
- C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C10/00—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
- C03C10/0054—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing PbO, SnO2, B2O3
-
- 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
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
Definitions
- the native metals cannot be used because of their hand ency to oxidize at temperatures below the normal operating temperature of the gas turbine engine, which may be as high as 1600 to 1800 F.
- molybdenum forms an oxide at about 1463 F. which sublimes, giving rise to a characteristic smoking of the metal which ultimately results in its disintegration.
- refractory metals such as molybdenum with other metals or metalloids
- these coatings have not proven to be satisfactory in all respects.
- conditions must be present such that a firm bond occurs between the coating metal and refractory base metal without too deep a penetration of the coating metal into the base metal.
- the coating must have thermal-shock resistance and must be impervious to oxygen and oxidizing gases.
- the coefiicient of thermal expansion of the coating metal must be equal to or slightly less than that of the refractory metal body. This latter condition is necessary so that the coating metal is always under a stress under operating conditions thus giving a much closer fit to the surface of the base metal.
- the coating metal must be non-volatile at the operating temperature of the engine, and maintain a good bond to the base metal.
- An object of the present invention is to provide a nonvolatile coating for molybdenum articles capable of forming a firm bond with the refractory metal, rendering the same impervious to oxygen and oxidizing gases.
- Another object of the present invention is to provide coatings for refractory metals which have coefficients of thermal expansion approximately equal to or slightly less than that of the refractory base metal.
- Another object of the invention is to provide a coating having the ability to reflect infrared radiation and thereby assist in cooling the body metal.
- a still further object of the invention is to provide a method for the production of a coated refractory metal having a high degree of hot strength and the ability to withstand corrosion at elevated temperatures.
- the invention comprises providing a coating for molybdenum articles by means of coating the same with a prefused mixture of alkaline earth aluminum silicates, plus modifying agents, substantially free from alkali metal compounds. It has been found that conventional glass compositions are not suitable for this purpose since they almost invariably contain some alkali metal compounds,
- Patented June 28, 1955 i. e., compounds of sodium and potassium, which are volatile at the operating temperature of the turbine engine.
- the volatilization of the oxides of the alkali metal decreases the ability of the coating to withstand corrosion to a very substantial degree.
- the refractory metal is provided with a coating consisting of a vitrified mixture containing about 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and l to 10% boric oxide.
- a preferred composition within the above range is one containing 10 to 20% calcium oxide, to 25% aluminum oxide, 50 to 60% silicon dioxide, and l to 10% boric oxide.
- boric oxide may be eliminated from the glass formula.
- boric oxide is included to bring the firing temperature down to the workable range. The firing temperature is an important consideration, and should be kept below 1900 F. to avoid impairing the physical properties of the molybdenum-base body.
- compositions may be added to the composition to enhance the properties of the final coating, as will be hereinafter more fully described.
- the method of the present invention is also applicable to alloys containing major proportions of molybdenum.
- the coatings may be applied to a molybdenum tungsten alloy containing up to about 5% tungsten.
- the body metal Prior to coating the molybdenum article with the vitreous coating, the body metal is worked to shape at appropriate forging temperatures.
- the properties of the article can be greatly enhanced by first pro-coating the worked refractory metal with a surface coating of metal or metalloid such as silicon, aluminum, or zirconium.
- a surface coating of metal or metalloid such as silicon, aluminum, or zirconium.
- this pre-coating is carried in the manner described in our copending application, Serial No. 98,272, filed June 10, 1949.
- the preferred glass compositions, according to the present invention have the following analyses, in percentages by weight:
- the boric oxide was included to promote melting and also to improve the thermal-shock resistance of the. glass. Boric oxide also helps to complex'the mixture so that a glass is actually formed. An amount of boric oxide up to about 10% has been found to be sufficient for this purpose.
- Zirconium oxide has the effect of increasing the viscosity of the glass.
- the oxide of zirconium will be included in the mill additions in an amount from about 5 to 30% by weight of the glass composition with parts per 100 parts of glass being the preferred amount.
- the particle size of the zirconium oxide added is preferably less than 5 or 6 microns.
- the procedure in applying the coating consists first of weighing and mixing the ingredients of the glass composition, and melting the batch at a temperature from about 2500 to 2700" F.
- the glass composition is fritted by pouring the molten mass into water.
- the glass is next ground while wet in ball mills or the like to a particle size of approximately 200 mesh, whereupon it is dried.
- the mill additions are weighed and added.
- These mill additions include refractory oxides, preferably zirconium oxide as mentioned above, together with binders and setting up agents.
- Typical mill additions which may be used are the various clays such as enamelers clay, bentonite, montmorillonite, Florida kaolin and the like.
- various metallic compounds such as chromium oxide, zinc oxide, cobalt oxide, nickel oxide, strontium oxide, iron oxide, manganese dioxide, calcium fluoride, and barium oxide may be added.
- the preferred setting up agent is methyl cellulose, since this agent has been found to increase the green film strength and reduce the tearing of the coat during firing.
- Methyl cellulose will be normally added in amounts up to about 1% with 0.1 part methyl cellulose per 100 parts glass being preferred.
- the various additives in the form of mill additions may be added in amounts from less than 1 part per 100 parts of glass, up to about parts per 100 parts of glass, exclusive of water.
- the amount of mill addition other than refractory oxides should be in the range from 0.01 and 4.0%.
- An eminently suitable coating composition may be prepared from the following formula:
- the article is then transferred to a furnace for the purpose of vitrifying the coating previously applied.
- a temperature in the range of about 1700 to 1900 F. is employed.
- the vitrifying step may be carried out in atmospheres ranging from slightly oxidizing, e. g., argon with a small amount of water vapor, through inert atmospheres, e. g., argon, helium, neon, krypton, to strongly reducing atmospheres, e. g., pure dry hydrogen.
- the baking is continued until a smooth vitrified coating is obtained.
- the thickness of the vitreous coating 7 will normally be from about 0.002 inch to 0.005 inch.
- Turbine buckets produced according to the the above disclosed process show remarkable ability to withstand corrosion.
- a turbine bucket pre-coated with silicon and coated with a vitrified coating of type disclosed above can withstand 1000 hours of operation at 1600 to 1800 F in air with no indication of failure.
- Articles coated according to the process of the present invention exhibit a high degree of thermal-shock resistance.
- the articles may be heated to red heat and water quenched without destroying the coating.
- the coatings are also extremely resistant ot oxygen and prevent passage of oxidizing gas into the base metal.
- the thermal expansion coefficient of the coating is somewhat less than that of the refractory metal base, so that a compression fit between the coating and the metallic base is effected under operating conditions.
- the coating also improves the damping capacity of the article.
- vitrified coating has the ability to refleet infra red radiations, as opposed to transmission. This reflection away from the body gives a substantial cooling effect to the article.
- non-volatile glass-like coatings form a smooth, firm bond to the surface of the molybdenum, or any pre-coat which has been applied thereto.
- a coated metal article comprising a base composed principally of molybdenum, and a corrosion resistant coating about said base consisting essentially of a vitrified mixture containing 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to silicon dioxide, 1 to 10% boric oxide, and 5 to 30% zirconium oxide, the thickness of said coating being on the order of .002 to .005 inch.
- the method of providing a corrosion resistant surface to molybdenum articles which comprises providing a shaped body composed principally of molybdenum, coating surfaces of the same with a glass composition consisting essentially of 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and 1 to 10% boric oxide, together with mill additions comprising zirconium oxide, said glass composition being substantially free of alkali metal compounds, and firing the coated article at a temperature suflicient to vitrify such coating.
- the method of providing a corrosion resistant surface to a molybdenum-base article which comprises providing a shaped body of molybdenum, coating surfaces of said body with a glass composition consisting essentially of 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and 1 to 10% boric oxide, together with mill additions comprising zirconium oxide, said glass composition being substantially free from alkali metal compounds, and firing the coated article in an atmosphere of inert gas at a temperature suflicient to vitrify said coating.
- the method of providing a corrosion resistant surface to a molybdenum-base article which comprises providing a shaped body of molybdenum, coating said shape with a surface layer of silicon, and coating surfaces of the thus coated shape with a glass composition consisting essentially of 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and l to 10% boric oxide, together with mil] additions comprising zirconium oxide, said glass composition being substantially free from alkali metal compounds, and firing the resulting coated article to a temperature sufficient to vitrify said coating.
- a ceramic composition for coating refractory metals consisting of a glass composition consisting essentially of 10 to calcium oxide, 10 to 30% aluminum oxide, to silicon dioxide and 1 to 10% boric oxide combined with mill additions containing zirconium oxide, said composition being capable of being fired into said refractory metal at a temperature in the range from 1700 to 1900 F.
- a coated metal article comprising a base of molybdenum, and a corrosion resistant ceramic coating over said base consisting essentially of a vitrified mixture of alkaline earth aluminum silicates together with mill additions comprising zirconium oxide.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Glass Compositions (AREA)
Description
VITREOUS C'QATEl) REFRACTORY METALS, METHOD FQR PRGDUCHJG THE S, AND VITREOUS ENAMEL CQMPOSITION Eugene Wainer and Robert A. Kempe, Cleveland, Ohio, assignors to Thompson Products, ind, Cleveland, Ohio, a corporation of Ohio No Drawing. Application July 1, 1949, Serial No. 102,708
6 Claims. or. 117-129 The manufacture of metals which have the ability to withstand the corrosive atmospheres present in gas turbines, while retaining their strength has always been a difiicult problem in jet engine manufacture. While metals such as molybdenum have good hot strength properties,
the native metals cannot be used because of their hand ency to oxidize at temperatures below the normal operating temperature of the gas turbine engine, which may be as high as 1600 to 1800 F. For example, molybdenum forms an oxide at about 1463 F. which sublimes, giving rise to a characteristic smoking of the metal which ultimately results in its disintegration.
While it has been previously suggested to coat refractory metals such as molybdenum with other metals or metalloids, these coatings have not proven to be satisfactory in all respects. in any such coating process, conditions must be present such that a firm bond occurs between the coating metal and refractory base metal without too deep a penetration of the coating metal into the base metal. Further, the coating must have thermal-shock resistance and must be impervious to oxygen and oxidizing gases. In addition, the coefiicient of thermal expansion of the coating metal must be equal to or slightly less than that of the refractory metal body. This latter condition is necessary so that the coating metal is always under a stress under operating conditions thus giving a much closer fit to the surface of the base metal. Probably the most important consideration in such a coating process is that the coating metal must be non-volatile at the operating temperature of the engine, and maintain a good bond to the base metal.
An object of the present invention is to provide a nonvolatile coating for molybdenum articles capable of forming a firm bond with the refractory metal, rendering the same impervious to oxygen and oxidizing gases.
Another object of the present invention is to provide coatings for refractory metals which have coefficients of thermal expansion approximately equal to or slightly less than that of the refractory base metal.
Another object of the invention is to provide a coating having the ability to reflect infrared radiation and thereby assist in cooling the body metal.
A still further object of the invention is to provide a method for the production of a coated refractory metal having a high degree of hot strength and the ability to withstand corrosion at elevated temperatures.
The invention comprises providing a coating for molybdenum articles by means of coating the same with a prefused mixture of alkaline earth aluminum silicates, plus modifying agents, substantially free from alkali metal compounds. It has been found that conventional glass compositions are not suitable for this purpose since they almost invariably contain some alkali metal compounds,
Patented June 28, 1955 i. e., compounds of sodium and potassium, which are volatile at the operating temperature of the turbine engine. The volatilization of the oxides of the alkali metal decreases the ability of the coating to withstand corrosion to a very substantial degree.
In particular, the refractory metal, according to the present invention, is provided with a coating consisting of a vitrified mixture containing about 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and l to 10% boric oxide. A preferred composition within the above range is one containing 10 to 20% calcium oxide, to 25% aluminum oxide, 50 to 60% silicon dioxide, and l to 10% boric oxide. Where the coating is fired at high temperatures, boric oxide may be eliminated from the glass formula. Where the coating is applied at lower temperatures, boric oxide is included to bring the firing temperature down to the workable range. The firing temperature is an important consideration, and should be kept below 1900 F. to avoid impairing the physical properties of the molybdenum-base body.
Various other materials may be added to the composition to enhance the properties of the final coating, as will be hereinafter more fully described.
The method of the present invention is also applicable to alloys containing major proportions of molybdenum. For example, the coatings may be applied to a molybdenum tungsten alloy containing up to about 5% tungsten.
Prior to coating the molybdenum article with the vitreous coating, the body metal is worked to shape at appropriate forging temperatures.
While the coating may be applied directly to the refractory metal, the properties of the article can be greatly enhanced by first pro-coating the worked refractory metal with a surface coating of metal or metalloid such as silicon, aluminum, or zirconium. Preferably this pre-coating is carried in the manner described in our copending application, Serial No. 98,272, filed June 10, 1949.
The preferred glass compositions, according to the present invention, have the following analyses, in percentages by weight:
Glass Component M N o. 2 N o. 3 N0. 4
In the above compositions the boric oxide was included to promote melting and also to improve the thermal-shock resistance of the. glass. Boric oxide also helps to complex'the mixture so that a glass is actually formed. An amount of boric oxide up to about 10% has been found to be sufficient for this purpose.
To reduce the firing temperature of a glass having a large refractory mill addition, minor amounts of compounds such as calcium fluoride, barium oxide and lithium oxide may be added. Examples of glass formulae which contain such additives are given below:
Glass Component Zirconium oxide has the effect of increasing the viscosity of the glass. The oxide of zirconium will be included in the mill additions in an amount from about 5 to 30% by weight of the glass composition with parts per 100 parts of glass being the preferred amount. The particle size of the zirconium oxide added is preferably less than 5 or 6 microns. Some zirconium goes into solution in the glass and serves to increase the toughness and hardness thereof. Zirconium oxide also increases the refractoriness and lowers the coefficient of expansion of the glass, thus providing an improved fit between the coating and the base.
The procedure in applying the coating consists first of weighing and mixing the ingredients of the glass composition, and melting the batch at a temperature from about 2500 to 2700" F. Next, the glass composition is fritted by pouring the molten mass into water. The glass is next ground while wet in ball mills or the like to a particle size of approximately 200 mesh, whereupon it is dried. Next, the mill additions are weighed and added. These mill additions include refractory oxides, preferably zirconium oxide as mentioned above, together with binders and setting up agents. Typical mill additions which may be used are the various clays such as enamelers clay, bentonite, montmorillonite, Florida kaolin and the like. In addition, various metallic compounds, such as chromium oxide, zinc oxide, cobalt oxide, nickel oxide, strontium oxide, iron oxide, manganese dioxide, calcium fluoride, and barium oxide may be added.
The preferred setting up agent is methyl cellulose, since this agent has been found to increase the green film strength and reduce the tearing of the coat during firing. Methyl cellulose will be normally added in amounts up to about 1% with 0.1 part methyl cellulose per 100 parts glass being preferred. The various additives in the form of mill additions may be added in amounts from less than 1 part per 100 parts of glass, up to about parts per 100 parts of glass, exclusive of water. The amount of mill addition other than refractory oxides should be in the range from 0.01 and 4.0%.
An eminently suitable coating composition may be prepared from the following formula:
Glass:
CaO per cent 15 A1203 do 20 SiOz do 60 B203 do 5 Mill formula:
Glass parts 100 ZrOz do 20 Methyl cellulose do 0.1 Water do 60 After the addition of the mill additions, the mixture is wetted and ground in a ball mill. Next, the glass is applied to the refractory metal article as by means of a spray gun.
The article is then transferred to a furnace for the purpose of vitrifying the coating previously applied. In baking the glass onto the surface of refractory metal precoated with a metal or metalloid of the type described previously, a temperature in the range of about 1700 to 1900 F. is employed. The vitrifying step may be carried out in atmospheres ranging from slightly oxidizing, e. g., argon with a small amount of water vapor, through inert atmospheres, e. g., argon, helium, neon, krypton, to strongly reducing atmospheres, e. g., pure dry hydrogen.
The baking is continued until a smooth vitrified coating is obtained. The thickness of the vitreous coating 7 will normally be from about 0.002 inch to 0.005 inch.
The above range for firing temperatures is employed where the article is to be used at high temperatures and under high stress, as for example, is the case in a turbine bucket. Where the article is to be used at high temperatures at relatively low stresses, this range may be exceeded.
Turbine buckets produced according to the the above disclosed process show remarkable ability to withstand corrosion. A turbine bucket pre-coated with silicon and coated with a vitrified coating of type disclosed above can withstand 1000 hours of operation at 1600 to 1800 F in air with no indication of failure.
Articles coated according to the process of the present invention exhibit a high degree of thermal-shock resistance. Thus, the articles may be heated to red heat and water quenched without destroying the coating.
The coatings are also extremely resistant ot oxygen and prevent passage of oxidizing gas into the base metal. The thermal expansion coefficient of the coating is somewhat less than that of the refractory metal base, so that a compression fit between the coating and the metallic base is effected under operating conditions. The coating also improves the damping capacity of the article.
In addition, the vitrified coating has the ability to refleet infra red radiations, as opposed to transmission. This reflection away from the body gives a substantial cooling effect to the article.
In addition, the non-volatile glass-like coatings form a smooth, firm bond to the surface of the molybdenum, or any pre-coat which has been applied thereto.
It will, of course, be understood that various details of the process may be varied through a wide range without departing from the principles of this invention and it is, therefore, not the purpose to limit the patent granted hereon otherwise than. necessitated by the scope of the appended claims.
We claim as our invention:
1. A coated metal article comprising a base composed principally of molybdenum, and a corrosion resistant coating about said base consisting essentially of a vitrified mixture containing 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to silicon dioxide, 1 to 10% boric oxide, and 5 to 30% zirconium oxide, the thickness of said coating being on the order of .002 to .005 inch.
2. The method of providing a corrosion resistant surface to molybdenum articles which comprises providing a shaped body composed principally of molybdenum, coating surfaces of the same with a glass composition consisting essentially of 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and 1 to 10% boric oxide, together with mill additions comprising zirconium oxide, said glass composition being substantially free of alkali metal compounds, and firing the coated article at a temperature suflicient to vitrify such coating.
3. The method of providing a corrosion resistant surface to a molybdenum-base article which comprises providing a shaped body of molybdenum, coating surfaces of said body with a glass composition consisting essentially of 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and 1 to 10% boric oxide, together with mill additions comprising zirconium oxide, said glass composition being substantially free from alkali metal compounds, and firing the coated article in an atmosphere of inert gas at a temperature suflicient to vitrify said coating.
4. The method of providing a corrosion resistant surface to a molybdenum-base article which comprises providing a shaped body of molybdenum, coating said shape with a surface layer of silicon, and coating surfaces of the thus coated shape with a glass composition consisting essentially of 10 to 30% calcium oxide, 10 to 30% aluminum oxide, 40 to 70% silicon dioxide, and l to 10% boric oxide, together with mil] additions comprising zirconium oxide, said glass composition being substantially free from alkali metal compounds, and firing the resulting coated article to a temperature sufficient to vitrify said coating.
5. A ceramic composition for coating refractory metals consisting of a glass composition consisting essentially of 10 to calcium oxide, 10 to 30% aluminum oxide, to silicon dioxide and 1 to 10% boric oxide combined with mill additions containing zirconium oxide, said composition being capable of being fired into said refractory metal at a temperature in the range from 1700 to 1900 F.
6. A coated metal article comprising a base of molybdenum, and a corrosion resistant ceramic coating over said base consisting essentially of a vitrified mixture of alkaline earth aluminum silicates together with mill additions comprising zirconium oxide.
References Cited in the file of this patent UNITED STATES PATENTS 2,421,719 Simmons June 3, 1947 5 FOREIGN PATENTS 214,492 Switzerland Apr. 30, 1941 OTHER REFERENCES High-Temperature Ceramic Coatings for Molybdenum, 19 Chemical and Engineering News, vol. 26, No. 45, No-
vember 8, 1948, pp. 3362-63.
Claims (1)
1. A COATED METAL ARTICLE COMPRISING A BASE COMPOUND PRINCIPALLY OF MOLYBDENIUM, AND A CORROSION RESISTANT COATINAG ABOUT SAID BASE CONSISTING ESSENTIALLY OF A VITRIFIED MIXTURE CONTAINING 10 TO 30% CALCIUM OXIDE, 10 TO 30% BORIC OXIDE, AND 5 TO 30% ZIRCONIUM OXIDE, THE THICKNESS OF SAID COATING BEING ON THE ORDER OF .002 TO .005 INCH.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US102708A US2711975A (en) | 1949-07-01 | 1949-07-01 | Vitreous coated refractory metals, method for producing the same, and vitreous enamel composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US102708A US2711975A (en) | 1949-07-01 | 1949-07-01 | Vitreous coated refractory metals, method for producing the same, and vitreous enamel composition |
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| Publication Number | Publication Date |
|---|---|
| US2711975A true US2711975A (en) | 1955-06-28 |
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| Application Number | Title | Priority Date | Filing Date |
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| US102708A Expired - Lifetime US2711975A (en) | 1949-07-01 | 1949-07-01 | Vitreous coated refractory metals, method for producing the same, and vitreous enamel composition |
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Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2825421A (en) * | 1953-10-02 | 1958-03-04 | Nelson Muffler Corp | Muffler |
| US2843500A (en) * | 1956-01-27 | 1958-07-15 | Cameron G Harman | Coated alloys |
| US2848349A (en) * | 1955-08-02 | 1958-08-19 | Armour Res Found | Flame spraying process |
| US2904449A (en) * | 1955-07-26 | 1959-09-15 | Armour Res Found | Method and compositions for flame spraying |
| US2977251A (en) * | 1956-11-21 | 1961-03-28 | Solar Aircraft Co | Protective coating methods and materials |
| US2985547A (en) * | 1958-06-13 | 1961-05-23 | Frenchtown Porcelain Company | Method for preparing coated bodies |
| US3019116A (en) * | 1957-10-11 | 1962-01-30 | Gen Electric | Ceramic body and method of making the same |
| US3121643A (en) * | 1955-03-23 | 1964-02-18 | Eisenberg Marvin | Flame spraying of oxidation-resistant, adherent coatings |
| US3222438A (en) * | 1959-02-27 | 1965-12-07 | Nat Res Dev | Heat resisting material and method for producing it |
| US3298860A (en) * | 1963-03-28 | 1967-01-17 | Ferro Corp | Coating metal with a clayless suspension of ceramic slips |
| US3420684A (en) * | 1964-06-19 | 1969-01-07 | Owens Illinois Inc | Sealing glass compositions,method of sealing,and article |
| US3443978A (en) * | 1964-08-14 | 1969-05-13 | Power Jets Res & Dev Ltd | Method of coating metals with a silicide layer and an outer layer of aluminasilicate |
| US5336453A (en) * | 1993-06-11 | 1994-08-09 | Aerospace Coating Systems, Inc. | Method for producing ceramic-based electronic components |
| US5603875A (en) * | 1993-06-11 | 1997-02-18 | Aerospace Coating Systems, Inc. | Method for producing ceramic-based components |
| US20120181725A1 (en) * | 2009-05-27 | 2012-07-19 | Lionel Montagne | Self-healing vitreous composition, method for preparing same, and uses thereof |
| US20130004633A1 (en) * | 2011-06-29 | 2013-01-03 | Link Forge Limited | Efficiency food smoker |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH214492A (en) * | 1938-07-07 | 1941-04-30 | Philips Nv | Process for melting an object consisting of molybdenum into glass, and a molybdenum object obtained by this process. |
| US2421719A (en) * | 1942-06-06 | 1947-06-03 | Western Electric Co | Vitreous enamelled article |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH214492A (en) * | 1938-07-07 | 1941-04-30 | Philips Nv | Process for melting an object consisting of molybdenum into glass, and a molybdenum object obtained by this process. |
| US2421719A (en) * | 1942-06-06 | 1947-06-03 | Western Electric Co | Vitreous enamelled article |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2825421A (en) * | 1953-10-02 | 1958-03-04 | Nelson Muffler Corp | Muffler |
| US3121643A (en) * | 1955-03-23 | 1964-02-18 | Eisenberg Marvin | Flame spraying of oxidation-resistant, adherent coatings |
| US2904449A (en) * | 1955-07-26 | 1959-09-15 | Armour Res Found | Method and compositions for flame spraying |
| US2848349A (en) * | 1955-08-02 | 1958-08-19 | Armour Res Found | Flame spraying process |
| US2843500A (en) * | 1956-01-27 | 1958-07-15 | Cameron G Harman | Coated alloys |
| US2977251A (en) * | 1956-11-21 | 1961-03-28 | Solar Aircraft Co | Protective coating methods and materials |
| US3019116A (en) * | 1957-10-11 | 1962-01-30 | Gen Electric | Ceramic body and method of making the same |
| US2985547A (en) * | 1958-06-13 | 1961-05-23 | Frenchtown Porcelain Company | Method for preparing coated bodies |
| US3222438A (en) * | 1959-02-27 | 1965-12-07 | Nat Res Dev | Heat resisting material and method for producing it |
| US3298860A (en) * | 1963-03-28 | 1967-01-17 | Ferro Corp | Coating metal with a clayless suspension of ceramic slips |
| US3420684A (en) * | 1964-06-19 | 1969-01-07 | Owens Illinois Inc | Sealing glass compositions,method of sealing,and article |
| US3443978A (en) * | 1964-08-14 | 1969-05-13 | Power Jets Res & Dev Ltd | Method of coating metals with a silicide layer and an outer layer of aluminasilicate |
| US5336453A (en) * | 1993-06-11 | 1994-08-09 | Aerospace Coating Systems, Inc. | Method for producing ceramic-based electronic components |
| US5603875A (en) * | 1993-06-11 | 1997-02-18 | Aerospace Coating Systems, Inc. | Method for producing ceramic-based components |
| US20120181725A1 (en) * | 2009-05-27 | 2012-07-19 | Lionel Montagne | Self-healing vitreous composition, method for preparing same, and uses thereof |
| US9160010B2 (en) * | 2009-05-27 | 2015-10-13 | Centre National De La Recherche Scientifique | Self-healing vitreous composition, method for preparing same, and uses thereof |
| US20130004633A1 (en) * | 2011-06-29 | 2013-01-03 | Link Forge Limited | Efficiency food smoker |
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