US3015579A - Metal coating process - Google Patents

Metal coating process Download PDF

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Publication number
US3015579A
US3015579A US820122A US82012259A US3015579A US 3015579 A US3015579 A US 3015579A US 820122 A US820122 A US 820122A US 82012259 A US82012259 A US 82012259A US 3015579 A US3015579 A US 3015579A
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Prior art keywords
metal
molybdenum
parts
pack
columbium
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US820122A
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Maurice R Commanday
James R Darnell
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Chromizing Corp
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Chromizing Corp
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C10/00Solid state diffusion of only metal elements or silicon into metallic material surfaces
    • C23C10/28Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
    • C23C10/34Embedding in a powder mixture, i.e. pack cementation
    • C23C10/58Embedding in a powder mixture, i.e. pack cementation more than one element being diffused in more than one step
    • 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
    • Y10S428/938Vapor deposition or gas diffusion
    • 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.]
    • Y10T428/12674Ge- or Si-base component
    • 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.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12806Refractory [Group IVB, VB, or VIB] metal-base component
    • Y10T428/12812Diverse refractory group metal-base components: alternative to or next to each other

Definitions

  • This invention has to do generally with improved surface treatments of the refractory metals columbium and tantalum to prevent their destructive oxidation when exposed to air at high temperatures, and to reduce their tendency toward embrittlement through the absorption of gases.
  • the refractory metals including also tungsten and molybdenum
  • the refractory metals can be rendered resistant to high temperature oxidation, by so-called siliconizing of the metal surfaces by either vapor phase (vapor plating) or solid pack techniques, according to which a silicon halide is caused to react with the metal surface to deposit silicon and form a coating complex that may be composed of silicon, silicides or silicon alloys of the base metal.
  • the pack method is advantageous over the vapor plating methods in that lower temperatures are employed, equipment is much simpler and more economical, continuou attendance of an operator is not required, and the size of the part that may be treated is not limited to the extent required in the vapor plating type of treatment.
  • the pack siliconizing process much greater dependency is placed upon reaction between the base metal and the active gases (silicon halide), and that the chemical properties of the base metal with respect to these gaseous components significantly aftect the result.
  • the silicon halide gas is believed to be reduced by hydrogen and deposited, as in the nature of electroplating, upon the base metal being treated, whereas in the packtype process, a reduction reaction or interchange reaction occurs.
  • molybdenum or ferro-molybdenum which may contain about 55 to 65% molybdenum and about 35 to 45% iron
  • This preliminary diffusion treatment produces what may be regarded as a primer coating of alloy rich molybdenum or molybdenum and iron, having peculiarly advantageous chemical properties for reaction with silicon halide gases in a subsequent pack siliconizing process to finally form a satisfactory protective coating.
  • the refractory base metal piece is first ferromolybdenumized by heating at a temperature in the range of about 1600 F. to 2800 F. for from 3 to 20 hours in a powder mixture composed of about 30 to 50 parts by weight of farm-molybdenum, 70 to 50 parts by weight of inert diluent, and about 0.02 to 5 parts of an inorganic halide, all solids being powdery and under about 60 mesh particle size.
  • the inert diluent may be any of various materials known to be usable in the solid pack type of treatment, such as tabular alumina, silica, bentonite, bauxite, kaolin, crushed fire clay, chromite and the like.
  • tabular alumina may be regarded as preferred.
  • the halogen-containing component may be any of the different inorganic halides such as the halides of iron, copper, or ammonia, the anionic halides of course being chlorine, bromine, fluorine and iodine. We prefer the use of the ammonium halides, and specifically ammonium bromide.
  • the pack method involves placement of the refractory metal piece or pieces to be treated, in surface contact with the powder mixture in an impermeable box or retort of an appropriate heat-resistant metal provided with a fusible rim seal that melts during the heating cycle to allow excess gase to vent, and which solidifies upon cooling to prevent air from entering the box.
  • an impermeable box or retort of an appropriate heat-resistant metal provided with a fusible rim seal that melts during the heating cycle to allow excess gase to vent, and which solidifies upon cooling to prevent air from entering the box.
  • the metal thus initially surface treated is removed from the pack and siliconized by a similar pack technique according to which the work metal is placed within the same kind of fusible rim box in contact with a powder mixture of from about 20 to 50 parts of silicon, 70 to 45 parts of inert filler such as tabular alumina, and 0.02 to 5 parts of an inorganic halide.
  • siliconizing of the previously treated metal surface results in the formation of a final coating on the base metal rendering the latter satisfactorily resistant to oxidation at high temperatures.
  • refractory metals treated in accordance with the invention we prepared three samples, the first being composed of 0.5 weight percent zirconium, and the balance columbium; a second containing 0.5 percent Zirconium, 39.5 percent tantalum and the balance columbium, and a third sample analyzing 16 percent molybdenum, 5.5 percent iron, 3.5 percent tantalum and the balance columbium. Specimens of each of these alloys were ferromolybdenumized by heating at 1900 F. for six hours in a powder mixture pack composed of 35 percent ferro-molybdenum (58.8% molybdenum and 41.2% iron), 65 percent tabular alumina and 0.3 percent ammonium bifluoride.
  • the ferromolybdenumized specimens were siliconized by heating at 1850 F. for eight hours in a powder pack mixture composed of 35 percent elemental silicon, about 65 percent tabular alumina and 0.3 percent ammonium bifluoride.
  • the specimens were subjected to static oxidation in air at 2400" F. with no observable breakdown of the coating or oxidation of the base metal, for periods up to one and one-half hours.
  • a refractory metal of the group consisting of colurnbium, tantalum and alloys thereof to render the metal surface resistant to oxidation at high temperatures, that includes, heating the metal to a temperature between about 1600 F. and 2800 F. in a non-oxidizing atmosphere and in surface contact with a powder mixture of about 30 to 50 weight parts of a substance of the class consisting of molybdenum and ferro molybdenum, about 70 to 50 parts of inert filler and 0.02 to parts of an inorganic halide and thereby alloying molybdenum into the metal surface; and subsequently heating the metal to a temperature between about 1600 F. and 2800 F.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)

Description

3,015,579 METAL COATING PRQCESS Rfaurice R. Commanday, Los Angeles, and James R.
Darnell, Reseda, Califi, assignors, by mesne assignments, to Chromizing Corporation, a corporation of Delaware No Drawing. Filed June 15, 1959, Ser. No. 820,122 8 Claims. (Cl. 117-107) This invention has to do generally with improved surface treatments of the refractory metals columbium and tantalum to prevent their destructive oxidation when exposed to air at high temperatures, and to reduce their tendency toward embrittlement through the absorption of gases.
It is well known in the art that the refractory metals, including also tungsten and molybdenum, can be rendered resistant to high temperature oxidation, by so-called siliconizing of the metal surfaces by either vapor phase (vapor plating) or solid pack techniques, according to which a silicon halide is caused to react with the metal surface to deposit silicon and form a coating complex that may be composed of silicon, silicides or silicon alloys of the base metal.
We have found that for our purposes the pack method is advantageous over the vapor plating methods in that lower temperatures are employed, equipment is much simpler and more economical, continuou attendance of an operator is not required, and the size of the part that may be treated is not limited to the extent required in the vapor plating type of treatment. We have also found that in the pack siliconizing process, much greater dependency is placed upon reaction between the base metal and the active gases (silicon halide), and that the chemical properties of the base metal with respect to these gaseous components significantly aftect the result. In vapor plating, the silicon halide gas is believed to be reduced by hydrogen and deposited, as in the nature of electroplating, upon the base metal being treated, whereas in the packtype process, a reduction reaction or interchange reaction occurs. As a consequence of this difference, we have found it dttlicult to achieve the highest success desired in the surface treating and coating of columbium and tantalum with simple pack siliconizing treatments, whereas similar techniques have proven quite satisfactory as applied to molybdenum and tungsten. Our general object in the present invention is to modify the surface of columbium or tantalum parts, so that they will be receptive to the pack siliconizing processes at practically desirable temperatures. In referring to the metals columbium and tantalum, we intend to also include their alloys, by which term i meant alloy compositions containing preponderantly the base metal together with any of other various metals depending upon the nature and properties of the alloy desired. For example such alloys may be composed of either columbium or tantalum together with lesser percentages of the other metals or such non-refractory metals as iron, nickel, chromium, zirconium and others.
In accordance with the invention we first difiuse molybdenum or ferro-molybdenum (which may contain about 55 to 65% molybdenum and about 35 to 45% iron), into the surface of the columbium or tantalum by means of a pack difiusion application preceding the siliconizing treatment. This preliminary diffusion treatment produces what may be regarded as a primer coating of alloy rich molybdenum or molybdenum and iron, having peculiarly advantageous chemical properties for reaction with silicon halide gases in a subsequent pack siliconizing process to finally form a satisfactory protective coating. The approach taken may appear unorthodox in that we employ the most reactive of all the refractory metals (molybdenum) insofar as its tendency for susceptibility to high nited States Patent temperature oxidation is concerned, to provide a basis for forming an oxidation-resistant coating on another refractory metal somewhat less prone to oxidation. However, the more active an element is in its pure state, generally the more stable are its compounds. Thus by surface alloying the less active element, e.g. columbium, with the more active element molybdenum, we are able to form more stable intermetallic compounds (molybdenum silicides) that exhibit superior protective properties, and do so by the simple solid pack process.
We have also found that the presence of iron in the primer coating tends to prevent embrittlement of the base metal, apparently due to absorption of gases during treatment or subsequent heating. This is particularly important in the instance of columbium, tantalum and their alloys, as room temperature ductility is a major advantage in these metals.
In more specific reference to the methods and materials employed in carrying out the invention, the refractory base metal piece is first ferromolybdenumized by heating at a temperature in the range of about 1600 F. to 2800 F. for from 3 to 20 hours in a powder mixture composed of about 30 to 50 parts by weight of farm-molybdenum, 70 to 50 parts by weight of inert diluent, and about 0.02 to 5 parts of an inorganic halide, all solids being powdery and under about 60 mesh particle size. The inert diluent may be any of various materials known to be usable in the solid pack type of treatment, such as tabular alumina, silica, bentonite, bauxite, kaolin, crushed fire clay, chromite and the like. For our purposes, tabular alumina may be regarded as preferred. The halogen-containing component may be any of the different inorganic halides such as the halides of iron, copper, or ammonia, the anionic halides of course being chlorine, bromine, fluorine and iodine. We prefer the use of the ammonium halides, and specifically ammonium bromide.
The pack method involves placement of the refractory metal piece or pieces to be treated, in surface contact with the powder mixture in an impermeable box or retort of an appropriate heat-resistant metal provided with a fusible rim seal that melts during the heating cycle to allow excess gase to vent, and which solidifies upon cooling to prevent air from entering the box. The physical characteristics of this type of pack have long been known in the art.
Following ferromolybdenumizing of the base metal as described, the metal thus initially surface treated is removed from the pack and siliconized by a similar pack technique according to which the work metal is placed within the same kind of fusible rim box in contact with a powder mixture of from about 20 to 50 parts of silicon, 70 to 45 parts of inert filler such as tabular alumina, and 0.02 to 5 parts of an inorganic halide. As heretofore indicated, siliconizing of the previously treated metal surface results in the formation of a final coating on the base metal rendering the latter satisfactorily resistant to oxidation at high temperatures.
As specific examples of refractory metals treated in accordance with the invention, we prepared three samples, the first being composed of 0.5 weight percent zirconium, and the balance columbium; a second containing 0.5 percent Zirconium, 39.5 percent tantalum and the balance columbium, and a third sample analyzing 16 percent molybdenum, 5.5 percent iron, 3.5 percent tantalum and the balance columbium. Specimens of each of these alloys were ferromolybdenumized by heating at 1900 F. for six hours in a powder mixture pack composed of 35 percent ferro-molybdenum (58.8% molybdenum and 41.2% iron), 65 percent tabular alumina and 0.3 percent ammonium bifluoride. Subsequently, the ferromolybdenumized specimens were siliconized by heating at 1850 F. for eight hours in a powder pack mixture composed of 35 percent elemental silicon, about 65 percent tabular alumina and 0.3 percent ammonium bifluoride. The specimens were subjected to static oxidation in air at 2400" F. with no observable breakdown of the coating or oxidation of the base metal, for periods up to one and one-half hours.
We claim:
1. The process of treating a refractory metal of the group consisting of colurnbium, tantalum and alloys thereof to render the metal surface resistant to oxidation at high temperatures, that includes, heating the metal to a temperature between about 1600 F. and 2800 F. in a non-oxidizing atmosphere and in surface contact with a powder mixture of about 30 to 50 weight parts of a substance of the class consisting of molybdenum and ferro molybdenum, about 70 to 50 parts of inert filler and 0.02 to parts of an inorganic halide and thereby alloying molybdenum into the metal surface; and subsequently heating the metal to a temperature between about 1600 F. and 2800 F. in a non-oxidizing atmosphere with said surface in contact with a powder mixture of about 20 to 50 parts of silicon, 70 to 45 parts of inert filler'and 0.02 to 5 parts of an inorganic halide to thereby form a molybdenum silicide protective surface coating.
2. The process of claim 1, in which said metal is columbium.
3. The process of claim 1, in which said metal is tantalum.
4. The process of claim 1, in which said ferromolybdenum contains about 55% to 65% molybdenum and about to iron.
5. The process of claim 1, in which said inert filler is alumina.
6. The process of claim 1, in which said halide is ammonium bromide.
7. The process of claim 1, in which said metal is columbium, said inert filler is alumina and said halide is ammonium bromide.
8. The product made according to the process of claim 1.
References Cited in the file of this patent UNITED STATES PATENTS 2,771,666 Campbell et a1. Nov. 27, 1956 2,825,658 Samuel Mar. 4, 1958 2,839,292 Bellamy June 17, 1958 2,876,139 Flowers Mar. 3, 1959 FOREIGN PATENTS 493,758 Canada June 16, 1953

Claims (1)

1. THE PROCESS OF TREATING A REFRACTORY METAL OF THE GROUP CONSISTING OF COLUMNIUM, TATALUM AND ALLOYS THEREOF TO RENDER THE METAL SURFACE RESISTANT TO OXIDATION AT HIGH TEMPERATURES, THAT INCLUDES, HEATING THE METAL TO A TEMPERSTURE BETWEEN ABOUT 1600* F. AND 2800* F. IN A NON-OXIDIZING ATMOSPHERE AND IN SURFACE CONTACT WITH A POWDER MIXTURE OF ABOUT 30 TO 50 WEIGHT PARTS OF A SUBSTANCE OF THE CLASS CONSISTING OF MOLYDDENUM AND FERRO MOLYBDENUM, ABOUT 70 TO 50 PARTS OF INERT FILLER AND 0.02 TO 5 PARTS OF AN INORGANIC HALIDE AND THEREBY ALLOYING MOLYBDENUM INTO THE METAL SURFACE; AND SUBSEQUENTLY HEATING THE METAL TO A TEMPERATURE BETWEEN ABOUT 1600* F.AND 2800* F. IN A NON-OXIDIZING ATMOSPHERE WITH SAID SURFACE IN CONTACT WITH A POWDER MIXTURE OF ABOUT 20 TO 5 PARTS OF AN INORGANIC HALIDE TO THEREBY FORM A MOLYBDENUM SILICIDE PROTECTIVE SURFACE COATING.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3293068A (en) * 1963-08-19 1966-12-20 United Aircraft Corp Coatings for columbium base alloys
US3293069A (en) * 1963-10-04 1966-12-20 United Aircraft Corp Coatings for columbium base alloys
US3337363A (en) * 1965-03-15 1967-08-22 Ritter Pfaudler Corp High temperature coatings for columbium alloys
US3383235A (en) * 1965-03-29 1968-05-14 Little Inc A Silicide-coated composites and method of making them
US3442720A (en) * 1965-10-23 1969-05-06 United Aircraft Corp Method of forming ti-modified silicide coatings on cb-base substrates and resulting articles
US3767456A (en) * 1971-09-07 1973-10-23 Fansteel Inc Chemical vapor deposition of steel with tantalum and columbium
US4369233A (en) * 1978-07-21 1983-01-18 Elbar B.V., Industrieterrien "Spikweien" Process to apply a protecting silicon containing coating on specimen produced from superalloys and product

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA493758A (en) * 1953-06-16 Metal-Gas Company Limited Treatment of metals
US2771666A (en) * 1950-03-18 1956-11-27 Fansteel Metallurgical Corp Refractory bodies
US2825658A (en) * 1954-10-04 1958-03-04 Metal Diffusions Inc Method of chromizing
US2839292A (en) * 1954-08-09 1958-06-17 Harry T Bellamy Refractory reservoir for aluminum
US2876139A (en) * 1956-06-27 1959-03-03 Gen Electric Method of bonding coating on a refractory base member and coated base

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA493758A (en) * 1953-06-16 Metal-Gas Company Limited Treatment of metals
US2771666A (en) * 1950-03-18 1956-11-27 Fansteel Metallurgical Corp Refractory bodies
US2839292A (en) * 1954-08-09 1958-06-17 Harry T Bellamy Refractory reservoir for aluminum
US2825658A (en) * 1954-10-04 1958-03-04 Metal Diffusions Inc Method of chromizing
US2876139A (en) * 1956-06-27 1959-03-03 Gen Electric Method of bonding coating on a refractory base member and coated base

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3293068A (en) * 1963-08-19 1966-12-20 United Aircraft Corp Coatings for columbium base alloys
US3293069A (en) * 1963-10-04 1966-12-20 United Aircraft Corp Coatings for columbium base alloys
US3337363A (en) * 1965-03-15 1967-08-22 Ritter Pfaudler Corp High temperature coatings for columbium alloys
US3383235A (en) * 1965-03-29 1968-05-14 Little Inc A Silicide-coated composites and method of making them
US3442720A (en) * 1965-10-23 1969-05-06 United Aircraft Corp Method of forming ti-modified silicide coatings on cb-base substrates and resulting articles
US3767456A (en) * 1971-09-07 1973-10-23 Fansteel Inc Chemical vapor deposition of steel with tantalum and columbium
US4369233A (en) * 1978-07-21 1983-01-18 Elbar B.V., Industrieterrien "Spikweien" Process to apply a protecting silicon containing coating on specimen produced from superalloys and product

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