US3449151A - Deposition of metal containing coating from vapor - Google Patents
Deposition of metal containing coating from vapor Download PDFInfo
- Publication number
- US3449151A US3449151A US473911A US3449151DA US3449151A US 3449151 A US3449151 A US 3449151A US 473911 A US473911 A US 473911A US 3449151D A US3449151D A US 3449151DA US 3449151 A US3449151 A US 3449151A
- Authority
- US
- United States
- Prior art keywords
- coating
- parts
- mixture
- aluminum
- metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000576 coating method Methods 0.000 title description 33
- 239000011248 coating agent Substances 0.000 title description 27
- 229910052751 metal Inorganic materials 0.000 title description 17
- 239000002184 metal Substances 0.000 title description 17
- 230000008021 deposition Effects 0.000 title description 2
- 239000000203 mixture Substances 0.000 description 33
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 18
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 15
- 238000000034 method Methods 0.000 description 15
- 229910052782 aluminium Inorganic materials 0.000 description 14
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 13
- 229910052804 chromium Inorganic materials 0.000 description 13
- 239000011651 chromium Substances 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 13
- 229910052759 nickel Inorganic materials 0.000 description 10
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 8
- 229940107816 ammonium iodide Drugs 0.000 description 8
- 238000005524 ceramic coating Methods 0.000 description 8
- 239000010955 niobium Substances 0.000 description 8
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 8
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000004901 spalling Methods 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910052790 beryllium Inorganic materials 0.000 description 3
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229910052715 tantalum Inorganic materials 0.000 description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- 239000010937 tungsten Substances 0.000 description 3
- 229910052720 vanadium Inorganic materials 0.000 description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- 229910000604 Ferrochrome Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910001026 inconel Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical class [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- -1 ammonium halide Chemical class 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000006060 molten glass Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
- C23C10/06—Solid state diffusion of only metal elements or silicon into metallic material surfaces using gases
- C23C10/14—Solid state diffusion of only metal elements or silicon into metallic material surfaces using gases more than one element being diffused in one step
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S252/00—Compositions
- Y10S252/95—Doping agent source material
- Y10S252/951—Doping agent source material for vapor transport
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/938—Vapor deposition or gas diffusion
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12472—Microscopic interfacial wave or roughness
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12674—Ge- or Si-base component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12729—Group IIA metal-base component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/12743—Next to refractory [Group IVB, VB, or VIB] metal-base component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12778—Alternative base metals from diverse categories
Definitions
- the present invention relates to a heat resistant, nonspalling ceramic coating for metal articles particularly parts having a relatively high percentage of chromium and/or nickel.
- Ceramic coating as defined herein refers to an essentially metal containing coating.
- a major drawback of ceramic coatings has been their low ductility which causes them to crack and to separate from thin sections of parts which flex during use, for instance due to vibration, and their tendency to spall when the part to which they are afiixed undergoes high amplitude temperature cycling such as is the case with jet engine combustion chambers, rocket nozzles and the like. Such spalling tendency is especially pronounced where the coatings must be relatively thick in order to protect the parts to which they are afiixed.
- An important object of the present invention is to provide a ceramic coating which is highly resistant to spalling and which coats metal parts uniformly even adjacent the edges and on thin sections thereof.
- Another object of the invention is the provision of a ceramic coating which has small grain size, is dense and uniform compared to prior art coatings.
- a further object of the present invention is the provision of a ceramic coating which penetrates relatively deeply into the coated part so as to be strongly adherent especially on such materials as Inconel; International Nickel Co. Alloy 713; nickel, aluminum, chromium and columbium bearing metals and steels.
- the parts to be coated are first degreased by immersion in a conventional degreasing solution, then are heated in a reducing atmosphere, for instance parts having a high chromium content may be heated in a hydrogen atmosphere.
- a reducing atmosphere for instance parts having a high chromium content may be heated in a hydrogen atmosphere.
- an exothermic gas such as dry, cracked illuminating gas or cracked ammonia gas could be utilized as the atmosphere.
- the heating step is preferably carried out at about 2150 degrees F. degrees F. for about one-half hour for the purpose of opening up the grain structure of the parts adjacent the exterior thereof in order to facilitate diffusion of the coating into the parts and to relieve my stresses.
- the parts are cooled in the reducing atmosphere to below 400 degrees F.
- the parts are next placed on suitable supports in a retort having means to facilitate the exit of gas therefrom and means to prevent the flow of air into the retort.
- Exemplary apparatus which per se, forms no part of the present invention includes an inverted cup-shaped drum inverted in a shallow saucer-like tray with a bed of powdered glass or the like in the tray surrounding the outside of the base of the cup-shaped drum.
- the parts are mounted on suitable racks in the upper part of the drum and the coating composition in the form of a powdered mixture and a catalyst to be described is disposed on the tray within the drum, below the parts.
- the glass powder in the moat surrounding the drum starts to melt and the coating composition mixture within the drum begins to sublime, pushing air out of the drum through the molten glass.
- the glass solidifies preventing entry of air into the retort as the parts cool.
- the parts cool in an air-free atmosphere.
- the mixture placed in the retort is composed of:
- the mixture is present as a powder of about 200 mesh.
- the coating of parts may be carried out at a temperature of 1700-2200 degrees F. and preferably is carried out at a temperature in the range between 1900 degrees F. and 2050 degrees F. inclusive.
- An increase in temperature and a lengthening of heating time increase the depth of the penetration.
- the coating increases in total depth by 0.002 inch per hour at 2000 degrees F.
- the parts are allowed to cool in a reducing atmosphere are then removed from the retort. No further processing of the coating is necessary.
- a specific example of a coating produced according to the present invention is on a part composed of, approximately 85% chromium and aluminum.
- the mixture in the retort comprised chromic oxide 60 percent, aluminum 38 percent and ammonium iodide 2.0 percent.
- the coating step was carried out in the gas phase at 2050 degrees F. for five hours.
- the uniform coating produced according to the present invention results in part because the coating is carried out by nascent attack in the gas phase wherein the iodide transports metal ions to the parts and the ammonia cracks to provide a reducing atmosphere.
- iodine will not cause burning of the parts or the coating at temperature above the coating range abovementioned and its low toxicity relative to the more reactive halides allows the ammonium iodide to be employed in a retort of the type described above whereas the use of chlorides, bromides or fluorides would necessitate using elaborate ventilation and accident prevention techniques.
- the chromic oxide can be replaced in whole or in part by oxides of tungsten, cobalt, columbium, molybdenum, nickel, silicon, tantalum, titanium, vanadium or zirconium and combinations thereof. Heating a mixture of berryllium fluoride and magnesium according to the conditions of the process described hereinabove will deposit a coating of beryllium and magnesium on the part that will withstand temperatures of about 2200 degrees F.
- the chromium and aluminum grains on the surface of parts coated according to the present invention tend to oxidize to form chromic and aluminum oxides. Because of the refractory character of these oxides, further burning is inhibited. Because of the extremely small grain size and spheroid shape of the coating, adherence is good, since expansion and contraction are allowed for. The brittle oxides, although adjacent to each other are not continuous and so cracking is prevented.
- a process for forming a nonspalling coating on a metallic part containing at least one constituent selected from the group consisting of chromium, nickel, aluminum, columbium and steel comprising:
- a reducing atmosphere is chosen from the group consisting of hydrogen, cracked illuminating gas or cracked ammonia.
- a process for forming a non-spalling coating on a metallic part containing at least one constituent selected from the group consisting of chromium, nickel, aluminum, columbium and steel comprising:
- said powdered mixture comprising at least one oxide of a metal selected from the group consisting of chromium, tungsten, cobalt, columbium, molybdenum, nickel, silicon, tantalum, titanium, vanadium, zirconium and mixtures thereof, a member selected from the group consisting of beryllium, magnesium and aluminum and a halogen containing sublimating agent and wherein the part is so disposed as to be out of physical contact with the said powder mixture;
- a powdered mixture for sublimation coating of metal parts consisting essentially of at least one metal oxide selected from the group consisting of chromium, tungsten, cobalt, columbium, molybdenum, nickel, silicon, tantalum, titanium, vanadium, zirconium and mixtures thereof, a member selected from the group consisting of beryllium, magnesium and aluminum and ammonium iodide.
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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)
- Powder Metallurgy (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Chemically Coating (AREA)
Description
United States Patent 3,449,151 DEPOSITION OF METAL CONTAINING COATING FROM VAPOR Howard D. Flicker, North Miami, Fla., assignor to Aircraft Plating Inc., Miami, Fla., a corporation of Florida No Drawing. Filed July 19, 1965, Ser. No. 473,911 Int. Cl. B44d 1/34; C23c 13/00, 1/08 U.S. Cl. 117-50 16 Claims ABSTRACT OF THE DISCLOSURE Disclosed is a method for forming a non-spalling coating upon a metal part by generating vapors from a pack containing a metal, metal oxide and ammonium halide and allowing the vapors to plate upon the metal part which is separated from the pack.
The present invention relates to a heat resistant, nonspalling ceramic coating for metal articles particularly parts having a relatively high percentage of chromium and/or nickel. Ceramic coating as defined herein refers to an essentially metal containing coating.
It is well known in the metallurgical field that the strength of alloys having a major percentage of steel diminishes with increase of temperature and walls off dramatically from 1400 to 1800 degrees F. This fact has limited the use of such materials to lower temperature applications and has required the development of alloys based on a major percentage of metals having better strength characteristics at higher temperatures such as columbium, nickel and chromium. Often metals having a relatively high heat resistance such as titanium have been used to coat less resistant metals. Such coatings tend to increase the heat resistance of the coated metal parts by 200 300 degrees F. or so but may be objectionable in certain applications because of their tendency to split away from the base metal and thus give the coated parts undesirable surface characteristics.
With the advent of jet and rocket engines where combustion chamber parts are heated to such levels that would cause unacceptable strength loss of steel alloy parts, the search for better coatings has been intensified, resulting in the development of many so-called ceramic coatings such as those which comprise chromium and iron as a solid solution on the surface of the parts being formed from a cementation pack mix of ferrochrome and kaolin. Surface roughness of the parts, alloying of the ferro-chrome with the metal of the part, as well as diffusion of the solution into the parts is relied on to adhere the coating to the parts.
A major drawback of ceramic coatings has been their low ductility which causes them to crack and to separate from thin sections of parts which flex during use, for instance due to vibration, and their tendency to spall when the part to which they are afiixed undergoes high amplitude temperature cycling such as is the case with jet engine combustion chambers, rocket nozzles and the like. Such spalling tendency is especially pronounced where the coatings must be relatively thick in order to protect the parts to which they are afiixed.
Many prior art ceramic coatings, such as those disclosed in the patent to Folliet et al., 1,943,171 are applied by embedding the part in a powdered mixture raising the temperature of the mixture and part in a container from which air is excluded. I have found that such coatings tend to be of uneven thickness and adherence and unacceptably rough for many applications absent additional surfaces finishing steps.
An important object of the present invention is to provide a ceramic coating which is highly resistant to spalling and which coats metal parts uniformly even adjacent the edges and on thin sections thereof.
Another object of the invention is the provision of a ceramic coating which has small grain size, is dense and uniform compared to prior art coatings.
A further object of the present invention is the provision of a ceramic coating which penetrates relatively deeply into the coated part so as to be strongly adherent especially on such materials as Inconel; International Nickel Co. Alloy 713; nickel, aluminum, chromium and columbium bearing metals and steels.
According to the present invention the parts to be coated are first degreased by immersion in a conventional degreasing solution, then are heated in a reducing atmosphere, for instance parts having a high chromium content may be heated in a hydrogen atmosphere. Alternatively, an exothermic gas such as dry, cracked illuminating gas or cracked ammonia gas could be utilized as the atmosphere.
The heating step is preferably carried out at about 2150 degrees F. degrees F. for about one-half hour for the purpose of opening up the grain structure of the parts adjacent the exterior thereof in order to facilitate diffusion of the coating into the parts and to relieve my stresses.
Following the heating step, the parts are cooled in the reducing atmosphere to below 400 degrees F. The parts are next placed on suitable supports in a retort having means to facilitate the exit of gas therefrom and means to prevent the flow of air into the retort. Exemplary apparatus which per se, forms no part of the present invention includes an inverted cup-shaped drum inverted in a shallow saucer-like tray with a bed of powdered glass or the like in the tray surrounding the outside of the base of the cup-shaped drum. The parts are mounted on suitable racks in the upper part of the drum and the coating composition in the form of a powdered mixture and a catalyst to be described is disposed on the tray within the drum, below the parts.
Upon heating the retort, the glass powder in the moat surrounding the drum starts to melt and the coating composition mixture within the drum begins to sublime, pushing air out of the drum through the molten glass. After the parts have been coated by the subliming mixture and heating of the retort is discontinued, the glass solidifies preventing entry of air into the retort as the parts cool. Thus, the parts cool in an air-free atmosphere.
According to the present invention, the mixture placed in the retort is composed of:
Preferably the mixture is present as a powder of about 200 mesh.
The coating of parts may be carried out at a temperature of 1700-2200 degrees F. and preferably is carried out at a temperature in the range between 1900 degrees F. and 2050 degrees F. inclusive. An increase in temperature and a lengthening of heating time increase the depth of the penetration. As an example, when parts of Inconel are being coated the coating increases in total depth by 0.002 inch per hour at 2000 degrees F.
Examination of the coatings produced by the present invention indicate that a reaction represented by the following equation predominates:
Substantial proportions of the metallic aluminum and of the metallic chromium diffuse into the surface region of the parts.
After the coating step, the parts are allowed to cool in a reducing atmosphere are then removed from the retort. No further processing of the coating is necessary.
A specific example of a coating produced according to the present invention is on a part composed of, approximately 85% chromium and aluminum. The mixture in the retort comprised chromic oxide 60 percent, aluminum 38 percent and ammonium iodide 2.0 percent. The coating step was carried out in the gas phase at 2050 degrees F. for five hours.
It appears that the uniform coating produced according to the present invention results in part because the coating is carried out by nascent attack in the gas phase wherein the iodide transports metal ions to the parts and the ammonia cracks to provide a reducing atmosphere. Unlike the more reactive halides, iodine will not cause burning of the parts or the coating at temperature above the coating range abovementioned and its low toxicity relative to the more reactive halides allows the ammonium iodide to be employed in a retort of the type described above whereas the use of chlorides, bromides or fluorides would necessitate using elaborate ventilation and accident prevention techniques.
In the coating mixture according to the present invention the chromic oxide can be replaced in whole or in part by oxides of tungsten, cobalt, columbium, molybdenum, nickel, silicon, tantalum, titanium, vanadium or zirconium and combinations thereof. Heating a mixture of berryllium fluoride and magnesium according to the conditions of the process described hereinabove will deposit a coating of beryllium and magnesium on the part that will withstand temperatures of about 2200 degrees F.
In use, the chromium and aluminum grains on the surface of parts coated according to the present invention tend to oxidize to form chromic and aluminum oxides. Because of the refractory character of these oxides, further burning is inhibited. Because of the extremely small grain size and spheroid shape of the coating, adherence is good, since expansion and contraction are allowed for. The brittle oxides, although adjacent to each other are not continuous and so cracking is prevented.
I claim:
1. A process for forming a nonspalling coating on a metallic part containing at least one constituent selected from the group consisting of chromium, nickel, aluminum, columbium and steel comprising:
placing the part to be coated and a powdered mixture in a container, said powdered mixture comprising chromic oxide, aluminum and ammonium iodide and wherein the part is so disposed as to be out of physical contact with the said powder mixture;
heating the part and the powdered mixture to a temperature in the range between 1700 and 2200 degrees F. whereby the mixture sublimes and condenses on the part forming a coating on said part,
allowing said part to cool in said container; and
removing said part from said container.
2. The process of claim 1 wherein the mixture is essentially composed of 60 weight percent chromic oxide, 38 Weight percent aluminum and 2.0 weight percent ammonium iodide.
3. The process of claim 1 wherein said temperature is in the range between 1900 and 2050 degrees F.
4. The process of claim 1 further comprising vdegreasing the part before the initial heating of the part in a reducing atmosphere.
5. The process of claim 1 wherein a reducing atmosphere is chosen from the group consisting of hydrogen, cracked illuminating gas or cracked ammonia.
6. The process of claim 1 wherein the ammonium iodide cracks during the said heating step and he Said I heating step and cooling step of the coated part are substantially carried out in the resulting reducing atmosphere. 7. The process of claim 1 wherein the said heating step and said cooling step of the coated part are carried out in a reducing atmosphere.
8. The process of claim 1 wherein the said coating step and said cooling step of the coated part are carried out in a substantially air-free atmosphere.
9. A process for forming a non-spalling coating on a metallic part containing at least one constituent selected from the group consisting of chromium, nickel, aluminum, columbium and steel comprising:
heating the part in a reducing atmosphere sufiiciently to open the grain structure of the part adjacent the exterior thereof, and subsequently cooling the part placing the part to be coated and a powdered mixture in a container, said powdered mixture comprising at least one oxide of a metal selected from the group consisting of chromium, tungsten, cobalt, columbium, molybdenum, nickel, silicon, tantalum, titanium, vanadium, zirconium and mixtures thereof, a member selected from the group consisting of beryllium, magnesium and aluminum and a halogen containing sublimating agent and wherein the part is so disposed as to be out of physical contact with the said powder mixture;
heating the part and the powdered mixture to a temperature in the range between 1700 and 2200 degrees F. whereby the mixture sublimes and condenses on the part forming a coating on said part, allowing said part to cool in said container; and removing said part from said container.
10. The process of claim 9 wherein the said coating step and said cooling step of the coated part are carried out in a substantially air-free atmosphere.
11. The process of claim 9 wherein the sublimating agent is ammonium iodide.
12. A metal part coated by the process of claim 9.
13. A powdered mixture for forming a coating on parts containing at least one of a constituent from the group consisting of chromium, nickel, aluminum, columbium and steel, said mixture consisting, essentially of chromic oxide; aluminum and ammonium iodide.
14. The mixture of claim 13 wherein the aluminum is finely divided beingof at least 200 mesh.
15. The mixture of claim 13 wherein the chromic oxide constitutes about 60 percent by weight of the mixture, aluminum about 38 percent by weight of the mixture and ammonium diode about 2.0 percent by weight of the mixture.
16. A powdered mixture for sublimation coating of metal parts, said powdered mixture consisting essentially of at least one metal oxide selected from the group consisting of chromium, tungsten, cobalt, columbium, molybdenum, nickel, silicon, tantalum, titanium, vanadium, zirconium and mixtures thereof, a member selected from the group consisting of beryllium, magnesium and aluminum and ammonium iodide.
References Cited UNITED STATES PATENTS 1,943,171 1/1934 Folliet.
2,274,671 3/1942 Daeves et al 117-22 3,123,493 3/1964 Brick 117-50 3,257,230 6/ 1966 Wachtell et al.
3,290,126 12/1966 Monson.
3,303,064 2/1967 Bernick et a1. 117-53 X ALFRED L. LEAVITI, Primary Examiner.
A. GOLIAN, Assistant Examiner.
US. 01. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47391165A | 1965-07-19 | 1965-07-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3449151A true US3449151A (en) | 1969-06-10 |
Family
ID=23881520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US473911A Expired - Lifetime US3449151A (en) | 1965-07-19 | 1965-07-19 | Deposition of metal containing coating from vapor |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3449151A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3535103A (en) * | 1968-04-10 | 1970-10-20 | Atomic Energy Commission | Method of making metal alloy powders |
| US4276088A (en) * | 1980-06-24 | 1981-06-30 | Zaets Inna I | Composition for diffusion coating of ferrous metals |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1943171A (en) * | 1929-10-30 | 1934-01-09 | Folliet Alexandre | Cementation mixture for ferrous metals |
| US2274671A (en) * | 1937-07-21 | 1942-03-03 | Daeves Karl | Formation of chromium-containing layers on ferrous surfaces |
| US3123493A (en) * | 1964-03-03 | Art of bonding of vacuum metallized coatings | ||
| US3257230A (en) * | 1964-03-24 | 1966-06-21 | Chromalloy American Corp | Diffusion coating for metals |
| US3290126A (en) * | 1965-04-29 | 1966-12-06 | Du Pont | Protectively coated nickel or cobalt articles and process of making |
| US3303064A (en) * | 1963-11-29 | 1967-02-07 | Inland Steel Co | Alloy steel article and method of producing |
-
1965
- 1965-07-19 US US473911A patent/US3449151A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3123493A (en) * | 1964-03-03 | Art of bonding of vacuum metallized coatings | ||
| US1943171A (en) * | 1929-10-30 | 1934-01-09 | Folliet Alexandre | Cementation mixture for ferrous metals |
| US2274671A (en) * | 1937-07-21 | 1942-03-03 | Daeves Karl | Formation of chromium-containing layers on ferrous surfaces |
| US3303064A (en) * | 1963-11-29 | 1967-02-07 | Inland Steel Co | Alloy steel article and method of producing |
| US3257230A (en) * | 1964-03-24 | 1966-06-21 | Chromalloy American Corp | Diffusion coating for metals |
| US3290126A (en) * | 1965-04-29 | 1966-12-06 | Du Pont | Protectively coated nickel or cobalt articles and process of making |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3535103A (en) * | 1968-04-10 | 1970-10-20 | Atomic Energy Commission | Method of making metal alloy powders |
| US4276088A (en) * | 1980-06-24 | 1981-06-30 | Zaets Inna I | Composition for diffusion coating of ferrous metals |
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