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 PDF

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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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Wainer Eugene
Robert A Kempe
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Northrop Grumman Space and Mission Systems Corp
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Thompson Products Inc
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    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • C03C3/093Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C10/00Devitrified 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
    • C03C10/0054Devitrified 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
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • Y10T428/263Coating 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)
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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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Cited By (16)

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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)

* Cited by examiner, † Cited by third party
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

Patent Citations (2)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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
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