US2952904A - Applying protective metal coatings on molybdenum - Google Patents

Applying protective metal coatings on molybdenum Download PDF

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US2952904A
US2952904A US634365A US63436557A US2952904A US 2952904 A US2952904 A US 2952904A US 634365 A US634365 A US 634365A US 63436557 A US63436557 A US 63436557A US 2952904 A US2952904 A US 2952904A
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molybdenum
layer
coating
brazing alloy
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Earl K Hann
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CBS Corp
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Westinghouse Electric Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/24Selection of soldering or welding materials proper
    • B23K35/30Selection of soldering or welding materials proper with the principal constituent melting at less than 1550 degrees C
    • B23K35/3033Ni as the principal constituent
    • B23K35/304Ni as the principal constituent with Cr as the next major constituent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/001Interlayers, transition pieces for metallurgical bonding of workpieces
    • B23K35/005Interlayers, transition pieces for metallurgical bonding of workpieces at least one of the workpieces being of a refractory metal
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/923Physical dimension
    • Y10S428/924Composite
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/923Physical dimension
    • Y10S428/924Composite
    • Y10S428/926Thickness of individual layer specified
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/934Electrical process
    • Y10S428/935Electroplating
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/936Chemical deposition, e.g. electroless plating
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/937Sprayed metal
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/939Molten or fused coating
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/94Pressure bonding, e.g. explosive
    • 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
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12632Four or more distinct components with alternate recurrence of each type component

Definitions

  • This invention relates to molybdenum metal with well bonded imperforate protective-metal coatings applied to the surface thereof.
  • Components suitablefor use as buckets, blades, valves, nozzles, and the like, in gas or steam turbines, jet engines and devices having similar atmosphere and temperature conditions, must possess high hot tensile strength, hot fatigue strength, and high resistance-to creep at elevated temperatures.
  • the refractory metal molybdenum possesses certain desirable characteristics which make it highly adaptable for structural materials exposed to high temperatures.
  • molybdenum is readily oxidized when exposed to an oxygen-bearing atmosphere at elevated temperatures.
  • molybdenum melts at 2625 C. in anon-oxidizing atmosphere if the molybdenum metal is heated to 500 C. and higher in contact with air, oxygen, or other oxidizing gas, it forms a readily volatile oxide.
  • a piece of the molybdenum metal gives oif dense dark clouds of smoke consisting ofmolybdenum oxides and in a short time it is consumed.
  • the molybdenum metal be provided with a coating of a metal resistant to oxidation at the elevated temperatures of use, but it is also essential ⁇ that the coating have good resistance to impace and shock under normally expected service conditions so as not to crack or spall and thereby expose the molybdenum body.
  • Aviation gas turbine engine components are often subject to impact and shock from foreign particles, such as pebbles and the like being picked up and passed through the engine at high velocity. Should the impact of the foreign particles cause the coating metal to crack, the molybdenum body would thus become .exposed to high temperature oxidation, this exposure resulting in premature failure of the component in service.
  • the thickness of the applied protective coating is critical in that it must be of such a thickness to possess high impact resistance and at the same time adequately accommodate for diiferences in thermal expansion between the protective coating and the molybdenum body.
  • the object of this invention is to provide a body of molybdenum metal with a well bonded imperforate coating having good resistance to oxidation at elevated tem peratures and good resistance to impact and shock, said coating comprising at least one layer of an oxidationresistant metal sandwiched between at least two layers of a fused brazing alloy.
  • Another object of the invention is to provide a body of molybdenum with an imperforate coating of critical thickness to enable it to meet impacts and shock Without being subject to failure due to differences in thermal expansion, said coating being bonded to the body of molybdenum by a nickel-chromium base brazing alloy.
  • Fig. l is a cross-section through a member comprising a body of molybdenum with an imperforate protective coating comprising three metal layers applied thereto;
  • Fig. 2 is a cross-section through a member comprising a body of molybdenum with an imperforate protective coating comprising tive metal layers applied thereto.
  • the method comprises applying to the molybdenum body a layer of a nely divided brazing alloy to a thickness of the order of from about 1/2 vmil to 2 mils and then heat-treating the molybdenum body with the applied brazing alloy to at least a temperature corresponding to the melting point of the brazing alloy -in a reducing atmosphere.
  • a relatively thin layer of the order of from about l mil to 3 mils of an oxidation-resistant metal is then applied to the entire surface of the fused brazing alloy.
  • a third layer of a thickness of the order of about 1/2 mil to 2 mils of the brazing alloy is then applied to the entire surface of the oxidation-resistant metal layer and heat-treated in the same manner as the first layer. Additional alternating layers of the oxidation-resistant metal and the brazing alloy can be applied if desired.
  • the rst layer that is applied to the body of molybdenum metal is a brazing alloy that is adherent to molybdenum and has good resistance to oxidation, said brazing alloy comprising, by weight, from 11% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to :i1/2% boron, and the balance being substantially all nickel with incidental impurities.
  • the layer of brazing alloy can be applied in any convenient manner. -It has been found that a convenient method of applying the layers of brazing alloy is to first prepare an aqueous slurry comprising calcium chloride and nely divided brazing alloy.
  • nely divided brazing alloy In preparing the slurry 12 parts to 55 parts by weight of nely divided brazing alloy is thoroughly admxed with each 10 parts by weight of a 10% aqueous calciumV chloride mixture. v'The brazing alloy passes through a sieve having from A100 to 300 meshes per inch. The slurry is applied to the molybdenum body by dipping or brushing methods. The molybdenum body Vwith the applied slurry is placed in a reducing'atmosphere-where' itis heated to a temperature corresponding at least to the liquidus or melting point of the brazing alloy for a period of time of from about 5 minutes to V15 minutes.
  • the brazing alloy fuses, thoroughly coats and firmly bonds tothe molybdenum body.
  • Y The calcium chloride serves as a ux during the-brazing operation. Caution Ymust be observed not Vto exceed too greatly the melting point vof the brazing alloy. If the melting point is greatly exceeded, thebrazing alloy will become too fluid and as a result will not be deposited in a Vlayer of uniform thickness over the entire surface of the molybdenum body, but will tend to flow oif elevated portions and gather at the bottom.
  • a temperature range of from about l050 C. to 11009 C. has been found to be a satisfactory melting range for the brazing alloys employed in this invention.
  • the oxidation-resistant layer can ⁇ be applied in any convenient manner. It is preferred, however, to apply chromium by electroplating means and to apply the chromium nickel alloys by Vspraying techniques or cladding methods.
  • the second oxidation-resistant layer is applied in a thickness of from l mil to 3 mils.
  • a third layer of a brazing alloy is then applied to the entire surface of the oxidation-resistant layer in the same manner as the rst layer of brazing alloy was applied to the molybdenum body.
  • the second application of fused brazing alloy serves to ill any pinholes that maybe present in the oxidation-resistant layer.
  • the molybdenum body is thus provided with a well bonded imperforate coating of a total thickness of about 5 mils comprising a layerof a thickness of from 1 mil to 3 mils of an oxidation-resistant metal sandwiched between two layers of fused brazing alloy.
  • an additional layer of an oxidation-resistant layer and an additional layer of fused brazing alloy can be applied so as to provide a coating comprising two layers of oxidation-resistant metal alternately sandwiched between three layers of fused brazing alloy.
  • both layers of oxidation-resistant metal be of the same composition or that they be applied in the same manner.
  • one layer could be electroplated chromium and the second layer could be sprayed chromium-nickel alloy.
  • the layers of fused brazing alloy be of the same composition.
  • the slurry is so applied as to provide on the entire surface of the member a layer of the slurry of a thickness of about 11/2 mils.
  • the coated molybdenum member is then placed in a furnace provided with a hydrogen atmosphere and is heated slowly to a temperature of l080 C. The temperature is held at 1080 C. for about 10 minutes. Heating is then terminated and the member Vcooled to room temperature in the hydrogen atmosphere.
  • the entire surface of the molybdenum member with the applied fused layer is removed from the furnace and spray coated by means of a flame spraying operation with an oxidation-resistant metal alloy comprising, by weight, %V nickel and 20% chromium. The alloy is applied in a thickness of about 2 mils.
  • a second layer of a thickness of about 2 mils of brazing alloy of the same composition as that of the rst applied layer is then applied to the entire surface of the oxidationresistant layer and fused-in a furnace in the same manner as the rst layer.
  • FIG. 1 of the drawing there is illustrated a cross section of a member produced in accordance with the process of thisV Example I.
  • the body 10 of molybdenum metal has applied to all of its surfaces a layer 12 of the fused brazing alloy.
  • the layer 12 has applied to all its surfaces a layer 14 of the 80% nickel, 20% chromium alloy, and to the layer 14 is applied a second layer 16 of the fused brazing alloy.
  • a ballistic impact test was carried out in which a test panel could be heated to elevated temperatures, then subjected to direct impact by copper vcoated steel pellets 0.175 inch in diameter projected at controllable muzzle velocity from ran air pistol with the muzzle .approximately 12 inches from the test panel which is held in position on a small anvil by clamping means.
  • Benjamin Air Pistol, Model -BB is held in position by wooden gun rests. The gun rests are vattached to the anvil by means of high temperature-resistant metal rods. The anvil with the attached test panel is placed in a furnace maintained at the test temperature. The pellets are fired at the test panel after the test panel has been heated to the desired temperature.
  • the following table shows the test results employing test panels prepared by coating a body of molybdenum 1 inch x 0.38 inch x 0.05 inch in accordance with Example I.
  • EXAMPLE II A member of molybdenum metal is sandblasted to clean and roughen the surface thereof.
  • An imperforate protective coating comprising ive layers, each averaging about 1.5 mils thick, is then applied in the following manner.
  • a first layer of fused brazing alloy comprising, by weight, 71.5% nickel, 11.5% chromium, 5.2% iron, 4.2% silicon, 2.5% boron, and 0.74% carbon, the balance being incidental impurities is 'applied to the entire surface of the molybdenum member in the same manner as set forth in Example I employing a slurry comprising 10 parts by weight of 10% aqueous calcium chloride and 35 parts by weight of the brazing alloy.
  • a third layer comprising the fused brazing alloy is applied to the entire surface of Y the second layer.
  • Another layer of clectrodeposited chromium is then applied to the entire surface of the third layer.
  • a final layer of the fused brazing alloy is applied to the entire surface of the second chromium layer.
  • Fig. 2 of the drawing there is illustrated a cross section of a member produced in accordance with the process of this example.
  • the body 20 of molybdenum metal has applied to all its surface a layer 22 of the fused brazing alloy.
  • the layer 22 has applied to all its surface a layer 24 of electrodeposited chromium to which is applied a second layer 26 of the fused brazing alloy.
  • a layer 28 of electrodeposited chromium has been applied to the entire surface of the layer 26.
  • a final layer 30 of the fused brazing alloy has been applied to the entire surface of the layer 28.
  • Molybdenum bodies coated in accordance with this invention have been subjected to continuous oxidation at temperatures up to 2000 F. for many hours without faiure. Furthermore, the coated molybdenum members of this invention have shown good results in thermal cycling test between room temperature and temperatures as high as 2000 F.
  • a member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising at least one continuous layer of an oxidation-resistant metal selected from the group consisting of chromium and nickel-chromium alloys sandwiched between at least two continuous layers of a fused brazing alloy comprising, by weight, from 11% to 25 chromium, from 2% to 12% silicon, up to 8% iron, up to 31/2% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused brazing alloy bonded together the layers to each other and to the molybdenum body, the said coating having a wall thickness of the order of from 5 mils to 10 mils.
  • a member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising at least two continuous layers of an oxidation-resistant metal, each of said layers being selected from the group consisting of chromium and nickelchromium alloys, alternately sandwiched between at least three continuous layers of a fused brazing alloy comprising, by weight, from ll% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to 31/2% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused brazing alloy bonding the layers to each other and to the molybdenum body and each of said layers being of a thickness of the order of from about 1/2 mil to 2 mils, each layer of said oxidation-resistant metal being of a thickness of the order of from about l
  • a member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising one continuous layer of a thickness of the order of from about l mil to 3 mils of an oxidation-resistant metal comprising, by weight, nickel and 20% chromium sandwiched between two continuous layers of a thickness of the order of from about 1/2 mil to 2 mils of a fused brazing alloy comprising, by weight, from 11% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to 31/2% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused brazing alloy bonding the layers to each other and to the molybdenum body, the total wall thickness of the layers being of the order of from 5 mils to 10 mils.
  • a member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising one continuous electrodeposited layer of a thickness of the order of from about 1 mil to 3 mils of chromium sandwiched between two continuous layers of a thickness of the order of from about 1/2 mil to 2 mils of a fused brazing alloy comprising, by weight, from 11% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to 31/z% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused metal alloy bonding the layers to each other and to the molybdenum body, the total wall thickness of the layers being of the order of from 5 mils to 10 mils.

Description

Sept. ZO, 1960 E. K. HANN 2,952,904
APPLYING PROTECTIVE METAL commes oN MOLYBDENUM Filed Jan. 15, 1957 Fig.
\l0 Molybdenum \2O Molybdenum 2B Electroploed Chromium WITNESSES INVENTORl Earl K. Honn United States Patent APPLYING PROTECTIVE METAL COA'I'INGS N MOLYBDENUM Earl K. Hann, Penn Township, Allegheny County, Pa., assignor to Westinghouse Electric Corporation, East Pittsburgh, Pa., a corporation of Pennsylvania Filed Jan. 15, 1957, Ser. No. '634,365
6 Claims. (Cl. 29-194) This invention relates to molybdenum metal with well bonded imperforate protective-metal coatings applied to the surface thereof.
Components suitablefor use as buckets, blades, valves, nozzles, and the like, in gas or steam turbines, jet engines and devices having similar atmosphere and temperature conditions, must possess high hot tensile strength, hot fatigue strength, and high resistance-to creep at elevated temperatures.
The refractory metal molybdenum possesses certain desirable characteristics which make it highly adaptable for structural materials exposed to high temperatures. However, molybdenum is readily oxidized when exposed to an oxygen-bearing atmosphere at elevated temperatures. Thus, while molybdenum melts at 2625 C. in anon-oxidizing atmosphere, if the molybdenum metal is heated to 500 C. and higher in contact with air, oxygen, or other oxidizing gas, it forms a readily volatile oxide. Thus, when in Contact with air at 700 C., for example, a piece of the molybdenum metal gives oif dense dark clouds of smoke consisting ofmolybdenum oxides and in a short time it is consumed.
It has been proposed to coat the surface of molybdenum metal with a protective layer of chromium or other oxidation-,resistant metal which would prevent access of oxygen or other oxidizing vapor to the molybdenum and in this way enable the use of molybdenum metal at temperatures above 500 C. It is absolutely necessary that such applied protective layers be imperferate in order to be of any Value. For example, electrodeposits of chromium have been plated on members of molybdenum and such coatings appeared to be sound and without pores. However, on heating such chromium plated member to 600 C. to 700 C., microscopic cracks and previously unnoted pinholes admitted oxygen to the molybdenum metal so that a stream of molybdenum oxide smoke issued from each of these Vopenings and in only a short time substantial volumes of the molybdenum metal adjacent to each such opening had disappeared because it had oxidized and the resulting volatile oxide had escaped.
For making components for high temperature applications as in gas turbines, jet engines and other highly heated applications demanding great strength, it is not only essential that the molybdenum metal be provided with a coating of a metal resistant to oxidation at the elevated temperatures of use, but it is also essential `that the coating have good resistance to impace and shock under normally expected service conditions so as not to crack or spall and thereby expose the molybdenum body. Aviation gas turbine engine components are often subject to impact and shock from foreign particles, such as pebbles and the like being picked up and passed through the engine at high velocity. Should the impact of the foreign particles cause the coating metal to crack, the molybdenum body would thus become .exposed to high temperature oxidation, this exposure resulting in premature failure of the component in service.
'2,952,904 Patented Sept. ,20, 1960 ice The thickness of the applied protective coating is critical in that it must be of such a thickness to possess high impact resistance and at the same time adequately accommodate for diiferences in thermal expansion between the protective coating and the molybdenum body.
The object of this invention is to provide a body of molybdenum metal with a well bonded imperforate coating having good resistance to oxidation at elevated tem peratures and good resistance to impact and shock, said coating comprising at least one layer of an oxidationresistant metal sandwiched between at least two layers of a fused brazing alloy.
Another object of the invention is to provide a body of molybdenum with an imperforate coating of critical thickness to enable it to meet impacts and shock Without being subject to failure due to differences in thermal expansion, said coating being bonded to the body of molybdenum by a nickel-chromium base brazing alloy.
Other objects of the invention will, in part, be obvious and will, yin part, appear hereinafter. For a better understanding of the nature and objects of the invention, reference should be had to the following detailed description and drawing, in which:
Fig. l is a cross-section through a member comprising a body of molybdenum with an imperforate protective coating comprising three metal layers applied thereto; and
Fig. 2 is a cross-section through a member comprising a body of molybdenum with an imperforate protective coating comprising tive metal layers applied thereto.
In accordance with this invention, a method has been discovered for producing on bodies of molybdenum metal, a highly protective surface coating of a critical thickness of the order of from 5 mils to l0 mils, which coating is highly resistant to impact and shock, and capable of accommodating differences in thermal expansion, and so Well bonded and adherent to the metal that it will withstand elevated temperatures for prolonged periods of time. Briefly, the method comprises applying to the molybdenum body a layer of a nely divided brazing alloy to a thickness of the order of from about 1/2 vmil to 2 mils and then heat-treating the molybdenum body with the applied brazing alloy to at least a temperature corresponding to the melting point of the brazing alloy -in a reducing atmosphere. A relatively thin layer of the order of from about l mil to 3 mils of an oxidation-resistant metal is then applied to the entire surface of the fused brazing alloy. A third layer of a thickness of the order of about 1/2 mil to 2 mils of the brazing alloy is then applied to the entire surface of the oxidation-resistant metal layer and heat-treated in the same manner as the first layer. Additional alternating layers of the oxidation-resistant metal and the brazing alloy can be applied if desired.
Y The invention will be detailed hereinafter specically by reference to molybdenum metal but it will be understood that similar procedures can be applied to temperature alloys in which molybdenum constitutes at leastv 50% by weight. Such alloys can comprise tungsten, niobium, and titanium as minor components. Thus, the invention can be applied to members comprising 99% molybdenum land 1% titanium.
The rst layer that is applied to the body of molybdenum metal is a brazing alloy that is adherent to molybdenum and has good resistance to oxidation, said brazing alloy comprising, by weight, from 11% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to :i1/2% boron, and the balance being substantially all nickel with incidental impurities. The layer of brazing alloy can be applied in any convenient manner. -It has been found that a convenient method of applying the layers of brazing alloy is to first prepare an aqueous slurry comprising calcium chloride and nely divided brazing alloy. In preparing the slurry 12 parts to 55 parts by weight of nely divided brazing alloy is thoroughly admxed with each 10 parts by weight of a 10% aqueous calciumV chloride mixture. v'The brazing alloy passes through a sieve having from A100 to 300 meshes per inch. The slurry is applied to the molybdenum body by dipping or brushing methods. The molybdenum body Vwith the applied slurry is placed in a reducing'atmosphere-where' itis heated to a temperature corresponding at least to the liquidus or melting point of the brazing alloy for a period of time of from about 5 minutes to V15 minutes. Forsmall components of an area of a` few ,square inches, such as jet engine blades, the heating ,time required Vis about minutes. The brazing alloy fuses, thoroughly coats and firmly bonds tothe molybdenum body. Y -The calcium chloride serves as a ux during the-brazing operation. Caution Ymust be observed not Vto exceed too greatly the melting point vof the brazing alloy. If the melting point is greatly exceeded, thebrazing alloy will become too fluid and as a result will not be deposited in a Vlayer of uniform thickness over the entire surface of the molybdenum body, but will tend to flow oif elevated portions and gather at the bottom. A temperature range of from about l050 C. to 11009 C. has been found to be a satisfactory melting range for the brazing alloys employed in this invention. v
A second layer of an oxidation-resistant metal selected from the-group consisting of chromium and chromiumnickel alloys melting above the melting point of the brazing alloy, is applied Vto the entire surface of the fused brazing alloy. The oxidation-resistant layer can `be applied in any convenient manner. It is preferred, however, to apply chromium by electroplating means and to apply the chromium nickel alloys by Vspraying techniques or cladding methods. The second oxidation-resistant layer is applied in a thickness of from l mil to 3 mils.
A third layer of a brazing alloy is then applied to the entire surface of the oxidation-resistant layer in the same manner as the rst layer of brazing alloy was applied to the molybdenum body. The second application of fused brazing alloy serves to ill any pinholes that maybe present in the oxidation-resistant layer. The molybdenum body is thus provided with a well bonded imperforate coating of a total thickness of about 5 mils comprising a layerof a thickness of from 1 mil to 3 mils of an oxidation-resistant metal sandwiched between two layers of fused brazing alloy.
If desired, an additional layer of an oxidation-resistant layer and an additional layer of fused brazing alloy can be applied so as to provide a coating comprising two layers of oxidation-resistant metal alternately sandwiched between three layers of fused brazing alloy. Also, it is not essential that both layers of oxidation-resistant metal be of the same composition or that they be applied in the same manner. For example, one layer could be electroplated chromium and the second layer could be sprayed chromium-nickel alloy. Further, it is not essential that the layers of fused brazing alloy be of the same composition.
The following examples illustrate the method of applying to a molybdenum body an imperforate protective coating in accordance with this invention.
EXAMPLE I A member of molybdenum metal is first sandblasted or otherwise treated to remove any impurities therefrom and also to roughen slightly the surface thereof. The entire surface of the molybdenum member is then brushed with a slurry of the following composition:
The slurry is so applied as to provide on the entire surface of the member a layer of the slurry of a thickness of about 11/2 mils. The coated molybdenum member is then placed in a furnace provided with a hydrogen atmosphere and is heated slowly to a temperature of l080 C. The temperature is held at 1080 C. for about 10 minutes. Heating is then terminated and the member Vcooled to room temperature in the hydrogen atmosphere. The entire surface of the molybdenum member with the applied fused layer is removed from the furnace and spray coated by means of a flame spraying operation with an oxidation-resistant metal alloy comprising, by weight, %V nickel and 20% chromium. The alloy is applied in a thickness of about 2 mils. A second layer of a thickness of about 2 mils of brazing alloy of the same composition as that of the rst applied layer is then applied to the entire surface of the oxidationresistant layer and fused-in a furnace in the same manner as the rst layer. v i
Referring to Fig. 1 of the drawing, there is illustrated a cross section of a member produced in accordance with the process of thisV Example I. The body 10 of molybdenum metal has applied to all of its surfaces a layer 12 of the fused brazing alloy. The layer 12 has applied to all its surfaces a layer 14 of the 80% nickel, 20% chromium alloy, and to the layer 14 is applied a second layer 16 of the fused brazing alloy.
A ballistic impact test was carried out in which a test panel could be heated to elevated temperatures, then subjected to direct impact by copper vcoated steel pellets 0.175 inch in diameter projected at controllable muzzle velocity from ran air pistol with the muzzle .approximately 12 inches from the test panel which is held in position on a small anvil by clamping means. Benjamin Air Pistol, Model -BB, is held in position by wooden gun rests. The gun rests are vattached to the anvil by means of high temperature-resistant metal rods. The anvil with the attached test panel is placed in a furnace maintained at the test temperature. The pellets are fired at the test panel after the test panel has been heated to the desired temperature. The following table shows the test results employing test panels prepared by coating a body of molybdenum 1 inch x 0.38 inch x 0.05 inch in accordance with Example I.
TableV I Test Panel Temperature Velocity of Results of Panel, F. Pellet, ft./'Sec.
1 1200 226 Continuous coating at impact area.
1200 341 Do. 1200 427 D0. .1500 226 D0. 1500 341 Do. 1500 I27 Do. 1800 226 Do. 1800 341 Do. 1800 427 Do.
EXAMPLE II A member of molybdenum metal is sandblasted to clean and roughen the surface thereof. An imperforate protective coating comprising ive layers, each averaging about 1.5 mils thick, is then applied in the following manner. A first layer of fused brazing alloy comprising, by weight, 71.5% nickel, 11.5% chromium, 5.2% iron, 4.2% silicon, 2.5% boron, and 0.74% carbon, the balance being incidental impurities is 'applied to the entire surface of the molybdenum member in the same manner as set forth in Example I employing a slurry comprising 10 parts by weight of 10% aqueous calcium chloride and 35 parts by weight of the brazing alloy. A second layer comprising chromiumvis ,then electrodeposited over the entire surface of the first layer. A third layer comprising the fused brazing alloy is applied to the entire surface of Y the second layer. Another layer of clectrodeposited chromium is then applied to the entire surface of the third layer. A final layer of the fused brazing alloy is applied to the entire surface of the second chromium layer.
Referring to Fig. 2 of the drawing, there is illustrated a cross section of a member produced in accordance with the process of this example. The body 20 of molybdenum metal has applied to all its surface a layer 22 of the fused brazing alloy. The layer 22 has applied to all its surface a layer 24 of electrodeposited chromium to which is applied a second layer 26 of the fused brazing alloy. A layer 28 of electrodeposited chromium has been applied to the entire surface of the layer 26. A final layer 30 of the fused brazing alloy has been applied to the entire surface of the layer 28.
'I'he following table shows the test results employing test panels prepared by coating a body of molybdenum 1 inch x 0.38 inch x 0.05 inch in accordance with It has been determined that the protective coatings of this invention should be at least about 5 mils in thickness so as to provide adequate resistance to impact. Furthermore, coatings of a thickness considerably in excess of mils, for example 30 mils, are too thick. Massive molybdenum bodies can be provided with thicker coatings than relatively small bodies, such as jet engine blades, without being subject to failure due to differences in thermal expansion.
Molybdenum bodies coated in accordance with this invention have been subjected to continuous oxidation at temperatures up to 2000 F. for many hours without faiure. Furthermore, the coated molybdenum members of this invention have shown good results in thermal cycling test between room temperature and temperatures as high as 2000 F.
Since certain obvious changes can be made in the above procedures and diiferent embodiments of the invention can be made without departing from the scope thereof, it is intended that all matter contained in the above description and drawing shall be interpreted as illustrative and not in a limiting sense.
I claim as my invention:
1. A member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising at least one continuous layer of an oxidation-resistant metal selected from the group consisting of chromium and nickel-chromium alloys sandwiched between at least two continuous layers of a fused brazing alloy comprising, by weight, from 11% to 25 chromium, from 2% to 12% silicon, up to 8% iron, up to 31/2% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused brazing alloy bonded together the layers to each other and to the molybdenum body, the said coating having a wall thickness of the order of from 5 mils to 10 mils.
2. A member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising at least two continuous layers of an oxidation-resistant metal, each of said layers being selected from the group consisting of chromium and nickelchromium alloys, alternately sandwiched between at least three continuous layers of a fused brazing alloy comprising, by weight, from ll% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to 31/2% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused brazing alloy bonding the layers to each other and to the molybdenum body and each of said layers being of a thickness of the order of from about 1/2 mil to 2 mils, each layer of said oxidation-resistant metal being of a thickness of the order of from about l mil to 3 mils, the said coating having a wall thickness of the order of from 5 mils to l0 mils.
3. A member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising one continuous layer of a thickness of the order of from about l mil to 3 mils of an oxidation-resistant metal comprising, by weight, nickel and 20% chromium sandwiched between two continuous layers of a thickness of the order of from about 1/2 mil to 2 mils of a fused brazing alloy comprising, by weight, from 11% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to 31/2% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused brazing alloy bonding the layers to each other and to the molybdenum body, the total wall thickness of the layers being of the order of from 5 mils to 10 mils.
4. The member of claim 3 wherein two continuous layers of the oxidation-resistant metal are alternately sandwiched between three continuous layers of the fused brazing alloy.
5. A member comprising a molybdenum body and a well bonded imperforate coating applied to the entire surface of the body, the coating having good resistance to oxidation at elevated temperatures and good resistance to impact and shock so as not to expose the molybdenum body under normally expected service conditions, said coating comprising one continuous electrodeposited layer of a thickness of the order of from about 1 mil to 3 mils of chromium sandwiched between two continuous layers of a thickness of the order of from about 1/2 mil to 2 mils of a fused brazing alloy comprising, by weight, from 11% to 25% chromium, from 2% to 12% silicon, up to 8% iron, up to 31/z% boron, and the balance being substantially all nickel with incidental impurities, said layers of fused metal alloy bonding the layers to each other and to the molybdenum body, the total wall thickness of the layers being of the order of from 5 mils to 10 mils.
6. 'Ihe member of claim 5 wherein two continuous electrodeposited layers of chromium are alternately sandwiched between three continuous layers of the fused brazing alloy.
References Cited in the le of this patent UNITED STATES PATENTS 2,247,755 Hensel July l, 1941 2,731,403 Rubin Jan. 17, 1956 2,739,107 Ricks Mar. 20, 1956 2,763,921 Turner Sept. 25, 1956 2,771,666 Campbell Nov. 27, 1956

Claims (1)

1. A MEMBER COMPRISING A MOLYBDENUM BODY AND A WELL BONDED IMPERFORATE COATING APPLIED TO THE ENTIRE SURFACE OF THE BODY, THE COATING HAVING GOOD RESISTANCE TO OXIDATION AT ELEVATED TEMPERATURES AND GOOD RESISTANCE TO IMPACT AND SHOCK SO AS NOT TO EXPOSE THE MOLYBDENUM BODY UNDER NORMALLY EXPECTED SERVICE CONDITIONS, SAID COATING COMPRISING AT LEAST ONE CONTINUOUS LAYER OF AN OXIDATION-RESISTANT METAL SELECTED FROM THE GROUP CONSISTING OF CHROMIUM AND NICKEL-CHROMIUM ALLOYS SANDWICHED BETWEEN AT LEAST TWO CONTINUOUS LAYERS OF A FUSED BRAZING ALLOY COMPRISING BY WEIGHT, FROM 11% TO 25% CHROMIUM, FROM 2% TO 12% SILICON, UP TO 8% IRON, UP TO 3 1/2% BORON, AND THE BALANCE BEING SUBSTANTIALLY ALL NICKEL WITH INCIDENTAL IMPURITIES, SAID LAYERS OF FUSED BRAZING ALLOY BONDED TOGETHER THE LAYERS TO EACH OTHER AND TO THE MOLYBDENUM BODY, THE SAID COATING HAVING A WALL THICKNESS OF THE ORDER OF FROM 5 MILS TO 10 MILS.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3112185A (en) * 1959-09-10 1963-11-26 Texas Instruments Inc Electron discharge devices and materials therefor
US3116981A (en) * 1960-03-17 1964-01-07 Edwin D Sayre Molybdenum and high temperature oxidation resistant alloy laminated composite material
US3122827A (en) * 1960-08-04 1964-03-03 Hughes Aircraft Co Polycrystalline article and method for making same
US3257703A (en) * 1961-09-29 1966-06-28 Texas Instruments Inc Composite electrode materials, articles made therefrom and methods of making the same
US3268362A (en) * 1961-05-26 1966-08-23 Rca Corp Deposition of crystalline niobium stannide
US3404968A (en) * 1964-09-30 1968-10-08 Westinghouse Electric Corp Glass-to-metal seals and method for making same

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2247755A (en) * 1940-02-03 1941-07-01 Mallory & Co Inc P R Electric contact
US2731403A (en) * 1952-11-08 1956-01-17 Pittsburgh Steel Co Manufacture of nickel-plated steel
US2739107A (en) * 1952-07-26 1956-03-20 Westinghouse Electric Corp Applying protective metal coatings on refractory metals
US2763921A (en) * 1952-01-24 1956-09-25 Thompson Prod Inc Corrosion and impact resistant article and method of making same
US2771666A (en) * 1950-03-18 1956-11-27 Fansteel Metallurgical Corp Refractory bodies

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2247755A (en) * 1940-02-03 1941-07-01 Mallory & Co Inc P R Electric contact
US2771666A (en) * 1950-03-18 1956-11-27 Fansteel Metallurgical Corp Refractory bodies
US2763921A (en) * 1952-01-24 1956-09-25 Thompson Prod Inc Corrosion and impact resistant article and method of making same
US2739107A (en) * 1952-07-26 1956-03-20 Westinghouse Electric Corp Applying protective metal coatings on refractory metals
US2731403A (en) * 1952-11-08 1956-01-17 Pittsburgh Steel Co Manufacture of nickel-plated steel

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3112185A (en) * 1959-09-10 1963-11-26 Texas Instruments Inc Electron discharge devices and materials therefor
US3116981A (en) * 1960-03-17 1964-01-07 Edwin D Sayre Molybdenum and high temperature oxidation resistant alloy laminated composite material
US3122827A (en) * 1960-08-04 1964-03-03 Hughes Aircraft Co Polycrystalline article and method for making same
US3268362A (en) * 1961-05-26 1966-08-23 Rca Corp Deposition of crystalline niobium stannide
US3257703A (en) * 1961-09-29 1966-06-28 Texas Instruments Inc Composite electrode materials, articles made therefrom and methods of making the same
US3404968A (en) * 1964-09-30 1968-10-08 Westinghouse Electric Corp Glass-to-metal seals and method for making same

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