US3338733A - Method of coating metallic surfaces with layers of nickel-chromium and aluminum - Google Patents
Method of coating metallic surfaces with layers of nickel-chromium and aluminum Download PDFInfo
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- US3338733A US3338733A US343174A US34317463A US3338733A US 3338733 A US3338733 A US 3338733A US 343174 A US343174 A US 343174A US 34317463 A US34317463 A US 34317463A US 3338733 A US3338733 A US 3338733A
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- nickel
- aluminum
- chromium
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- 238000000576 coating method Methods 0.000 title claims description 99
- 239000011248 coating agent Substances 0.000 title claims description 92
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 50
- 229910052782 aluminium Inorganic materials 0.000 title claims description 47
- 238000000034 method Methods 0.000 title claims description 15
- 229910018487 Ni—Cr Inorganic materials 0.000 title description 10
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 title description 10
- 230000007797 corrosion Effects 0.000 claims description 36
- 238000005260 corrosion Methods 0.000 claims description 36
- 229910045601 alloy Inorganic materials 0.000 claims description 32
- 239000000956 alloy Substances 0.000 claims description 32
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 30
- 229910000623 nickel–chromium alloy Inorganic materials 0.000 claims description 30
- 229910052751 metal Inorganic materials 0.000 claims description 29
- 239000002184 metal Substances 0.000 claims description 29
- 238000010438 heat treatment Methods 0.000 claims description 16
- 229910052759 nickel Inorganic materials 0.000 claims description 14
- 239000011651 chromium Substances 0.000 claims description 12
- 229910052804 chromium Inorganic materials 0.000 claims description 11
- 238000005507 spraying Methods 0.000 claims description 11
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 9
- 239000010953 base metal Substances 0.000 description 21
- 238000009792 diffusion process Methods 0.000 description 19
- 239000000126 substance Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 230000006698 induction Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000003754 machining Methods 0.000 description 4
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000005238 degreasing Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000011253 protective coating Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000005422 blasting Methods 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000003483 aging Methods 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 238000005269 aluminizing Methods 0.000 description 1
- 239000006079 antiknock agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- UOUJSJZBMCDAEU-UHFFFAOYSA-N chromium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Cr+3].[Cr+3] UOUJSJZBMCDAEU-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- -1 nickel chromium aluminum Chemical compound 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Images
Classifications
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- 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
- C23C10/28—Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
-
- 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/08—Metallic material containing only metal elements
-
- 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/18—After-treatment
-
- 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
- Y10S428/923—Physical dimension
- Y10S428/924—Composite
- Y10S428/926—Thickness of individual layer specified
-
- 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
- Y10S428/937—Sprayed metal
-
- 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
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12944—Ni-base component
Definitions
- the present invention relates to metallic surface coatings that are resistant to corrosion and wear at elevated temperatures and to an improved process for applying and bonding said surface coatings to metallic objects.
- one object of this invention is to provide a metal article having an improved metallic coating tenaciously bonded thereto that is resistant to corrosion at elevated tempera-tures.
- Another object of this invention is to provide a metal article having an improved metallic coating tenaciously bonded thereto that is extremely hard and resistant to corrosion and wear at elevated temperatures.
- Still another object of this invention is to provide a simple process whereby metallic objects of various coniigurations, including sheets, strips, rods, bars, irregularshaped bodies and the like can be quickly coated with corrosion and wear-resistant metals over all or a portion of the surface of said objects and tenaciously bonded thereto.
- FIGURE 1 is a magnified longitudinal sectional View of a fragmentary portion of the base metal having on its surface a coating of nickel-chromium alloy which is tenaciously bonded thereto by means -of an interdiiused chemical bond; and
- FIGURE 2 is a magnified longitudinal sectional view of a fragmentary portion of the base metal having on its surface an outer coat-ing of aluminum which has been interdiffused with the underlying coating of nickel-chromium alloy.
- the surface coating treatment is comprised of two separable treating sequences; first, the application and bonding of a corrosion-resistant coating to the base metal and, second, the application and interdiffusion of an aluminum coating over said corrosionresistant coating.
- the separability of these two treating sequences provides processing flexibility so that metal objects may be processed in only the rst or in both treating sequences, depending upon the extent and nature of the surface protection required.
- the corrosion-resistant coating sequence is comprised principally of the following processing steps: preheating the article to be coated ,to an elevated temperature, metal spraying the surface or a designated portion thereof with a corrosion-resistant metal alloy, and interdiffusing the coating and the base metal at an elevated temperature.
- the coated article may be surface finished if the texture and/ or dimensional tolerances of the coated article are critical.
- the sec-ond coating sequence is comprised principally of preheating the coated object, applying a thin coating of aluminum over the underlying corrosion-resistant coating, and iinally interdiffusing the aluminum coating with the underlying corrosion-resistant coating under controlled conditions.
- Application of the aluminum should be made on 4a metallurgically clean surface which may require a degreasing processing step prior to the preheat step. It may lalso be desirable, depending on the nature of the coated article, to perform a very light surface finishing operation on the overlying aluminum coating.
- the object to be treated may be of any metallic composition, providing, however, that the material is suliiciently resistant to corrosion so that substantially no oxide is formed on the surface thereof during the rapid pre-heat in air prior to applying the corrosion-resistant coating.
- the material is suliiciently resistant to corrosion so that substantially no oxide is formed on the surface thereof during the rapid pre-heat in air prior to applying the corrosion-resistant coating.
- ferrous base and nickel base stainless alloys that are resistant to oxide formation when rapidly heated in air to temperatures between about 1300 and 1800" F. and are suitable for surface treatment in accordance with this invention. Rapid heating techniques, such as induction heating, minimize surface oxidation because of the short length of time required to attain the desired temperature Iand consequently constitute the preferred heating method.
- the corrosion-resistant coating is applied to the base metal
- a second surface cleaning step, comprised of sand or grit blasting the surface is also preferred, in order to remove therefrom any solid deposits and oxide scales and impart a plurality of slight depressions in the surface of the base metal to -aid mechanical bonding of the initial surface coating prior to the diffusion step.
- the metal article with a metallurgically clean surface is next preheated rapidly to a temperature ranging between 1300 and 1800 F., preferably 1650 to 1800 F.
- Preheating the metal article prior to coating insures intimate contact of the corrosion-resistant coating with the surface of the base metal and improves mechanical bonding therebetween by preventing rapid cooling and contraction of the coating relative to the base surface.
- Attempts to apply a corrosion-resistant coating of an appreciable thickness such as 0.010 inch and thicker by metal spraying a metal article which had not been preheated resulted in extremely poor adherence and even complete separation of the coating from the surface.
- moderate preheat temperatures of about 800 F. failed to provide suicient adherence whereby adequate bonding might be achieved during the subsequent diffusion step. It is for this reason that preheat temperatures of at least 1300 F. are employed, and preferably 1650 F.
- a substantially pure 80 nickel 20 chromiu-m alloy is used, having a composition, for example, such as that specified in ASTM designation BSZ-57 adopted in 1946 and as revised in 1952 and in 1957, having an analysis as follows:
- a nickelchromium alloy can be utilized -having a broader composition range than the alloy specified above.
- the initial coating should consist substantially of a nickel-chromium alloy containing between 70 and 97 percent nickel and from 3 to 30 percent chromium with other constituents such as iron, cobalt and tungsten not to exceed a combined total of 10 percent by weight.
- Conventional quantities of age hardening elements, such as titanium, aluminum and molybdenum are not objectionable.
- elements such as boron forming low melting point oxides on the surface to be coated are undesirable.
- the nickelchromium alloy is applied by a metal spray technique utilizing Iconventional spray guns adaptable for melting and spraying nickel-chromium alloy supplied in a wire form.
- these spray guns utilize a combustible gas such as acetylene mixed with oxygen for converting the nickel-chromium wire into a molten state and in which state it is propelled in the form of fine droplets by an air blast toward the object to be coated.
- a coating of substantially uniform thickness ranging from about 0.1001 to 0.100 inch is applied to all or a designated portion of the surface of the preheated metal article.
- the nature of the bond between the Icoating and the base metal immediately after spraying is primarily a mechanical one comprised of interlocking surface irregularities and the bond is susceptible to rupture if subjected to high stresses.
- the coated metal object is next treated in a diffusion step wherein the mechanical bond is converted to a chemical bond which tenaciously secures the coating to the surface of the base material.
- the diffusion step is comprised of heating the coated metal object to a temperature between 1800 and 2250o F., preferably 1900 to 2100 F.
- interdiifusion or alloying occurs between the coating metal and the base metal to the depth of at least one atomic layer.
- the rate of interdifusion between the nickel-chromium alloy coating and base metal increases with temperature and, accordingly, the length of treatment time required to secure a satisfactory bond is inversely proportional to the temperature employed. Interdiifusion at a temperature of about 1800" F. is feasible but commercially undesirable because time periods as long as one hour are required to achieve satisfactory bonding of the coating to the base metal. On the other hand, diffusion at temperatures in excess of 2250 F.
- FIG- URE 1 An illustration of the relationship between a base metal 10 coated with a corrosion-resistant nickel-chromium alloy lll and tenaciously bonded thereto is shown in FIG- URE 1.
- the interdiffused chemical bond between the base metal 10 and corrosion-resistant coating 11 has been exaggerated for purposes of clarity and is indicated by the bond 12.
- the penetration or depth of the interdiifused zone 12. to achieve adequate chemical bonding should be at least one atomic layer and, preferably, about 0.0005 inch.
- Metallic articles coated with the nickel-chromium alloy and processed in accordance with the steps described above may be used in that form or, if smooth surfaces and dimensional tolerances are critical, the article may be surface :finished by machining, grinding, polishing or the like.
- the second coating treatment comprising the application of an overlying aluminum coating would sequentially follow the application and bonding of the nickel-chromium surface coating.
- the aluminum coating Prior to applying the aluminum coating, it may be necessary to re-clean the surface of the coated object, particularly if an intervening machining operation has been performed on the nickel-chromium surface coating.
- Preheating the metal article prior to the application of the aluminum coating is not absolutely essential, nor is it as critical as in the case of the preheat step preceding the application of the nickel-chrominum alloy coating. Generally, it is preferred to preheat the object to a temperature between 300 and 1400 F.
- the aluminum coating may be applied in a number of different ways, such as by dipping in a molten bath or, preferably, by the metallizing spray gun technique in a manner similar to that employed in applying the nickel-chromium alloy coating.
- the thickness of the aluminum spray coating may range from 0.0003 to 0.004 inch.
- a coating thickness of less than 0.0003 inch may not provide a sufficient quantity of aluminum to form analuminum nickel chromium alloy layer of sufficient thickness to provide the necessary protection, 'while a coating thickness exceeding 0.004 inch causes excessive flow and dripping of the aluminum coating during diffusion.
- Adherence of the aluminum to the nickelchromium alloy coating prior to the diffusion step is a combination of mechanical as well as chemical bonding.
- the rate of diffusion of aluminum into the nickel-chomi- Aum alloy coating is substantially greater that that of the nickel-chromium alloy into the base metal, so that at elevated preheat temperatures of about 1200 to l400 F. some interdiffusion occurs during the application of the aluminum to the metal article.
- the coated object is heated to a temperature within the range of from 1500 to 2100 F. and maintained at that temperature for a period of from a few seconds to five minutes to achieve controlled diffusion and alloying of the aluminum into the nickel-chromium alloy coating and forming therewith an extremely hard corrosionand wear- Vresistant coating.
- the diffusion time required is depend- 'ent on the diffusion temperature, as well as the preheat temperature of the metallic object during the spray ap- "plication of the aluminum. If, for example, the aluminum is applied to the coated object, pre-heated to a temperature of about l400 F., a substantial interdiffusion is achieved during the application of the aluminum with a lesser amount of subsequent diffusion required.
- the thickness of the interdiffused layer should be at least about 0.0003 inch thick to provide sufficient protection but, preferably, not greater than 0.004 inch thick, because of the brittle nature of the interdiffused alloy.
- FIGURE 2 An enlarged fragmentary view of a base metal having 'thereon an 'interdiffused alloy layer of aluminum, nickel and chromiumrisshown'in FIGURE 2.
- the diffused alloy layer is designated by the numeral 13 while the undiffused outer layer comprised predominantly of aluminum and oxides thereof is designated 14.
- the undiifused portion of the underlying nickel-chromium alloy coating 11 is bonded to the base metal 10 by means of chemical bond 12. It will, of course, be appreciated that the principal zones or layers on the surface of the base metal are not as definitive as shown in FIGURE 2, but rather, in actual practice, the layers gradually blend one into the other vwithout a definite line of demarcation.
- Hardness determinations lobtained with a Rockwell testing apparatus of the interdiffused alloy layer indicate the hardness to range from approximately 48 to 62 Rockwell C.
- X-ray diffraction analyses made of the composition of this unique corrosionand wear-resistant layer produced varying diffraction patterns, indicating that the alloy lacks chemical homogeneity. These X-ray studies further indicated that the predominant phase in the hard alloy layer is based on the space lattice Al3(Ni,Cr)2.
- the coating contains appreciable quantities of a second phase comprised of aluminum oxide in the form A1203 in amounts up to about l0 weight percent.
- the aluminum oxide as well as lesser quantities of nickel and chromium oxides are formed during the spray application of the coatings and during subsequent diffusions at elevated temperatures 1n air.
- One of the specific applications of this invention relates to the corrosion and wear protection of engine valves, particularly the exhaust valves of an internal combustion engine.
- gasolines inherently contain constituents such as sulfur which, on combustion, produce corrosive elements such as sulfur dioxide which have a deleterious effect on the metal objects they contact.
- most gasolines also contain small quantities of special additives, such as tetraethyl lead, as an anti-knock agent, halogenated hydrocarbons as scavengers for the lead oxide formed from tetra- -ethyl lead during combustion, and phosphorus-containing compounds to inhibit pre-ignition and spark plug fouling.
- additives although effective to achieve their intended purpose, are highly corrosive and attack the surface of engine valves exposed tothe high temperature exhaust gases with a resultant pitting and flaking of the valve, materially shortening its effective operating life.
- engine valves can be produced which are highly resistant to corrosion and Wear under these severe operating conditions.
- Most engine valves are of a ferrous or nickel base stainless alloy having, the requisite oxidation resistance suitable for applying the nickel-chromium alloy coating in accordance with the processing sequence heretofore described.
- iron oxide formation on the head face of the valve promotes pre-ignition, a Very damaging form of combustion.
- a coating of nickel-chromium alloy over the head portion of the valve exposed to the high temperature exhaust gases is sufficient to prevent formation of the' iron oxide scale.
- the seat face of the valve is, of course, that portion of the valve which is in contact with the valve seat, forming therewith a pressure-tight seal.
- a typical processing sequence for applying a corrosionand wear-resistant coating to the base of a valve is comprised of taking the valve that has been machined roughly to size and cleaning the surface to be coated by degreasing and grit blasting.
- the cleaned valve is next inserted so that its head is surrounded by an induction coil providing localized heating, whereby the surface to be coated is raised to a temperature of approximately 1700 F. within about fifteen seconds and a nickel-chromium alloy sprayed on the face of said valve immediately after its withdrawal from the coil.
- the head of the valve is reinserted in the induction coil and heated to a diffusion temperature of approximately 2100 F. for a period of about one minute, and then permitted to cool gradually in air prior to machining.
- the head is reinserted in an induction coil, whereby it is preheated to approximately 500 F. in a matter of seconds, and then withdrawn from the coil to permit an aluminum sprayy coating to be applied over the nickel-chromium alloy coating.
- T he coated valve is once again reinserted into the induction coil and heated to a temperature of about 2000 F. for a period of approximately four minutes to provide controlled interdiffusion of the aluminum and nickel-chromium alloy coating forming thereby the corrosion and wear resistant layer having a hardness in the range of about 48 to 58 Rockwell C.
- the valve is then permitted to cool gradually in air to room temperature, at which time it is ready for use.
- Variations to this processing sequence include the application of the nickel-chromium corrosion-resistant alloy to the head as Well as to the seat face of the valve in cases where head corrosion protection is also desired.
- a protective coating of aluminum on the head portion of the valve which may be either uncoated or coated with the nickel-chromium alloy and in which case it is preferred to dip the entire head of the valve in a bath of molten aluminum.
- the individual treating steps are, of course, adaptable to integration by automation whereby the metallic article or valve to be coated can be automatically processed starting with the uncoated object through to the nished product.
- a process for applying a coating on at least a portion of a metallic surface comprising the l.steps of preheating said surface in air to a temperature in the range of about 1300 to about 1800e F., metal spraying at least a portion of the metallurgically clean preheated surface with an alloy containing at least weight percent of the elements nickel and chromium, said nickel content ranging from about 97 to about 70 Weight percent, said chromium content ranging from abou 3 to about 30 weight percent, heating said coated ⁇ surface to a temperature in the range of about 1800 to about 2250 F.
- a process for applying a coating on at least a portion of a metallic surface comprising the steps of preheating said surface in air to a temperature in the range of about 1300 to about 1800 F., metal spraying at least a portion of the metallurgically clean preheated surface with an alloy containing at least 90 weight percent of the elements nickel and chormium, said nickel content rang- Iing from about 97 to about 70* weight percent, said chromium content ranging from about 3 to about 30 weight percent, heating said coated surface to a temperature in the range of about 1800 to about 2250 F.
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Description
Aug. 29, 1967 E. P. R-OWADY 3,338,733
METHOD OF' COATING METALLIC SURFACES WITH LAYERS OF NICKEIJCHROMIUM AND ALUMINUM Original Filed `June: 26, 1959 //fused M' -Cr and base mem/j 1N VEN TOR. IIa/4r] 7? Fa wat@ (Eas mefa/) I United States Patent O 3,338,733 METHD F COATING METALLIC SURFACES WITH LAYERS 0F NICKEL-CHROMIUM AND ALUMINUM Edward P. Rowady, Detroit, Mich., assigner to Eaton Yale & Towne Inc., a corporation of Delaware Original application .lune 26, 1959, Ser. No. 823,214, now Patent No. 3,165,823, dated Jan. 19, 1965, Divided and this application Dec. 30, 1963, Ser. No. 343,174
2 Claims. (Cl. 117-50) This application is a division of application Ser. No. 823,214, led June 26, 1959 and now U.S. Patent, 3,165,823 issued Jan. 19, 1965.
The present invention relates to metallic surface coatings that are resistant to corrosion and wear at elevated temperatures and to an improved process for applying and bonding said surface coatings to metallic objects.
A great number of applications exist wherein metallic articles are subjected at elevated temperatures to corrosive gases, such as air, and combustion gases resulting from the burning of a variety of fuels. Under these conditions, articles composed of metals such as iron and many ferrous base alloys, that are susceptible to such corrodents are severely attacked on their surfaces as evidenced by pitting and surface scaling and this surface deterioration materially reduces their operating etiiciency and useful life. This condition is further aggravated when the objects must concurrently withstand surface to surface contact and wear, particularly when operating tolerances between said adjacent surfaces are critical. Substitution of corrosion susceptible base metals with special heat-resistant alloys to achieve a satisfactory operating life has not been entirely satisfactory because of the greater cost of such special alloys, which are generally more diicult to manufacture and to fabricate into the desired form. Quite often, the substitution of special corrosion-resistant alloys results in a sacrifice or compromise of some of the structural considerations in favor of the corrosion-resistant properties of the material. Numerous surface coatings have been applied to base metals susceptible to corrosion at elevated temperatures to obviate the necessity of substituting special heat-resistant alloys and to achieve a satisfactory operating life of the metal object. However, the processes by which surface coatings have been heretofore applied have been commercially undesirable due to their complexity, prolonged treating cycle and resultant uneconomical operation.
Accordingly, one object of this invention is to provide a metal article having an improved metallic coating tenaciously bonded thereto that is resistant to corrosion at elevated tempera-tures.
Another object of this invention is to provide a metal article having an improved metallic coating tenaciously bonded thereto that is extremely hard and resistant to corrosion and wear at elevated temperatures.
Still another object of this invention is to provide a simple process whereby metallic objects of various coniigurations, including sheets, strips, rods, bars, irregularshaped bodies and the like can be quickly coated with corrosion and wear-resistant metals over all or a portion of the surface of said objects and tenaciously bonded thereto.
Other objects and advantages of the present invention will vbecome apparent from the following detailed description taken in `conjunction with the accompanying drawings, wherein:
FIGURE 1 is a magnified longitudinal sectional View of a fragmentary portion of the base metal having on its surface a coating of nickel-chromium alloy which is tenaciously bonded thereto by means -of an interdiiused chemical bond; and
FIGURE 2 is a magnified longitudinal sectional view of a fragmentary portion of the base metal having on its surface an outer coat-ing of aluminum which has been interdiffused with the underlying coating of nickel-chromium alloy.
The surface coating treatment, as embodied in this invention, is comprised of two separable treating sequences; first, the application and bonding of a corrosion-resistant coating to the base metal and, second, the application and interdiffusion of an aluminum coating over said corrosionresistant coating. The separability of these two treating sequences provides processing flexibility so that metal objects may be processed in only the rst or in both treating sequences, depending upon the extent and nature of the surface protection required. The corrosion-resistant coating sequence is comprised principally of the following processing steps: preheating the article to be coated ,to an elevated temperature, metal spraying the surface or a designated portion thereof with a corrosion-resistant metal alloy, and interdiffusing the coating and the base metal at an elevated temperature. Because superior bonding of the coating if achieved when the article has a metallurgically clean surface, appropriate surface cleaning steps should precede the preheating and coating steps. In addition, the coated article may be surface finished if the texture and/ or dimensional tolerances of the coated article are critical. The sec-ond coating sequence is comprised principally of preheating the coated object, applying a thin coating of aluminum over the underlying corrosion-resistant coating, and iinally interdiffusing the aluminum coating with the underlying corrosion-resistant coating under controlled conditions. Application of the aluminum should be made on 4a metallurgically clean surface which may require a degreasing processing step prior to the preheat step. It may lalso be desirable, depending on the nature of the coated article, to perform a very light surface finishing operation on the overlying aluminum coating.
The object to be treated may be of any metallic composition, providing, however, that the material is suliiciently resistant to corrosion so that substantially no oxide is formed on the surface thereof during the rapid pre-heat in air prior to applying the corrosion-resistant coating. There are numerous ferrous base and nickel base stainless alloys that are resistant to oxide formation when rapidly heated in air to temperatures between about 1300 and 1800" F. and are suitable for surface treatment in accordance with this invention. Rapid heating techniques, such as induction heating, minimize surface oxidation because of the short length of time required to attain the desired temperature Iand consequently constitute the preferred heating method.
With reference to the iirst treating sequence wherein the corrosion-resistant coating is applied to the base metal, it is preferred to clean the article in a Vapor degreasing operation or other suitable cleaning operation, to remove any surface film which may have been deposited thereon, such as during prior handling or in machining operations. A second surface cleaning step, comprised of sand or grit blasting the surface is also preferred, in order to remove therefrom any solid deposits and oxide scales and impart a plurality of slight depressions in the surface of the base metal to -aid mechanical bonding of the initial surface coating prior to the diffusion step.
The metal article with a metallurgically clean surface is next preheated rapidly to a temperature ranging between 1300 and 1800 F., preferably 1650 to 1800 F.
for Imost materials, which constitutes a critical step of this process. Preheating the metal article prior to coating insures intimate contact of the corrosion-resistant coating with the surface of the base metal and improves mechanical bonding therebetween by preventing rapid cooling and contraction of the coating relative to the base surface. Attempts to apply a corrosion-resistant coating of an appreciable thickness such as 0.010 inch and thicker by metal spraying a metal article which had not been preheated resulted in extremely poor adherence and even complete separation of the coating from the surface. Moreover, the use of moderate preheat temperatures of about 800 F. failed to provide suicient adherence whereby adequate bonding might be achieved during the subsequent diffusion step. It is for this reason that preheat temperatures of at least 1300 F. are employed, and preferably 1650 F. to l800 F. Preheat temperatures in excess of 1800 F. are undesirable because of the increasing tendency to form oxides on the surface to be coated. As heretofore mentioned, the use of rapid heating techniques such as induction heating, which constitutes a preferred heating method, generally requires only a fraction of a minute to elevate the object to be coated to the appropriate temperature. When that` temperature has been attained, a metal coating of corrosion-resistant alloy is immediately applied over all or that portion of the surface `of the -metal object that `requires protection.
In surface treating applications wherein only the first treating sequence is to be utilized, a substantially pure 80 nickel 20 chromiu-m alloy is used, having a composition, for example, such as that specified in ASTM designation BSZ-57 adopted in 1946 and as revised in 1952 and in 1957, having an analysis as follows:
Element: Weight percent Nickel 77-'79 Chromium 19-20 Iron, maximum l Manganese, maximum 2.5 Carbon, maximum 0.25 Silicon 0.75- Sulphur, maximum 0.03
The presence of other elements in the alloy that have a tendency to form low melting point oxides such as the element boron, for example, which reduce the overall melting temperature of the oxide on the surface of the metal object are undesirable constituents because they accelerate the normal corrosion rate.
In surface treatments which include both the treating sequences, that is, the corrosion-resistant coating followed by an valuminum coating, a nickelchromium alloy can be utilized -having a broader composition range than the alloy specified above. The initial coating should consist substantially of a nickel-chromium alloy containing between 70 and 97 percent nickel and from 3 to 30 percent chromium with other constituents such as iron, cobalt and tungsten not to exceed a combined total of 10 percent by weight. Conventional quantities of age hardening elements, such as titanium, aluminum and molybdenum are not objectionable. As aforementioned, elements such as boron forming low melting point oxides on the surface to be coated are undesirable.
In the preferred practice of this invention, the nickelchromium alloy is applied by a metal spray technique utilizing Iconventional spray guns adaptable for melting and spraying nickel-chromium alloy supplied in a wire form. Generally, these spray guns utilize a combustible gas such as acetylene mixed with oxygen for converting the nickel-chromium wire into a molten state and in which state it is propelled in the form of fine droplets by an air blast toward the object to be coated. In this manner, a coating of substantially uniform thickness ranging from about 0.1001 to 0.100 inch is applied to all or a designated portion of the surface of the preheated metal article. The nature of the bond between the Icoating and the base metal immediately after spraying is primarily a mechanical one comprised of interlocking surface irregularities and the bond is susceptible to rupture if subjected to high stresses. For the purpose of obtaining an improved bond, the coated metal object is next treated in a diffusion step wherein the mechanical bond is converted to a chemical bond which tenaciously secures the coating to the surface of the base material. To avoid rupture of the aforementional interlocking surface irregularities, it is preferred to prevent the coated metal object from cooling rapidly to a temperature substantially below the preheat temperature prior to the diffusion step. The diffusion step is comprised of heating the coated metal object to a temperature between 1800 and 2250o F., preferably 1900 to 2100 F. for a short duration of time so that interdiifusion or alloying occurs between the coating metal and the base metal to the depth of at least one atomic layer. The rate of interdifusion between the nickel-chromium alloy coating and base metal increases with temperature and, accordingly, the length of treatment time required to secure a satisfactory bond is inversely proportional to the temperature employed. Interdiifusion at a temperature of about 1800" F. is feasible but commercially undesirable because time periods as long as one hour are required to achieve satisfactory bonding of the coating to the base metal. On the other hand, diffusion at temperatures in excess of 2250 F. occurs rapidly, requiring a treating period of only about a minute or less, but this temperature is unsatisfactory because of the rapid growth in the grain size of the base metal and the tendency to oxidize any exposed surface of a metallic object which may have received a protective coating over only a portion of its surface. Furthermore, warping of the metal object at very high temperatures may occur and, of course, melting of the base metal is the final limiting factor. For these reasons, in the prefer-red practice of this invention, diffusion temperatures of 1900 to 2100 F. are employed, requiring treating periods of from about one to about iive minutes for producing tenaciously bonded nickelchromium alloy coatings.
An illustration of the relationship between a base metal 10 coated with a corrosion-resistant nickel-chromium alloy lll and tenaciously bonded thereto is shown in FIG- URE 1. The interdiffused chemical bond between the base metal 10 and corrosion-resistant coating 11 has been exaggerated for purposes of clarity and is indicated by the bond 12. As has heretofore been mentioned, the penetration or depth of the interdiifused zone 12. to achieve adequate chemical bonding should be at least one atomic layer and, preferably, about 0.0005 inch.
Metallic articles coated with the nickel-chromium alloy and processed in accordance with the steps described above may be used in that form or, if smooth surfaces and dimensional tolerances are critical, the article may be surface :finished by machining, grinding, polishing or the like.
In situations where, in addition to the nickel-chromium corrosion-resistant coating, it is desired to impart a hard, corrosionand wear-resistant coating to the metal object the second coating treatment comprising the application of an overlying aluminum coating would sequentially follow the application and bonding of the nickel-chromium surface coating. Prior to applying the aluminum coating, it may be necessary to re-clean the surface of the coated object, particularly if an intervening machining operation has been performed on the nickel-chromium surface coating. Preheating the metal article prior to the application of the aluminum coating is not absolutely essential, nor is it as critical as in the case of the preheat step preceding the application of the nickel-chrominum alloy coating. Generally, it is preferred to preheat the object to a temperature between 300 and 1400 F. to remove all traces of moisture on the surface of the object and to facilitate intimate Contact between the aluminum and the nickel-chromium intermediate coating. Although a commercially pure aluminum is preferred, such as a 2S grade, alloys of aluminum with elements such as silicon, copper and magnesium in percentages preferably not exceedingfa combined total of l percent by weight are also satisfactory. The aluminum coating may be applied in a number of different ways, such as by dipping in a molten bath or, preferably, by the metallizing spray gun technique in a manner similar to that employed in applying the nickel-chromium alloy coating. The thickness of the aluminum spray coating may range from 0.0003 to 0.004 inch. A coating thickness of less than 0.0003 inch may not provide a sufficient quantity of aluminum to form analuminum nickel chromium alloy layer of sufficient thickness to provide the necessary protection, 'while a coating thickness exceeding 0.004 inch causes excessive flow and dripping of the aluminum coating during diffusion. Adherence of the aluminum to the nickelchromium alloy coating prior to the diffusion step is a combination of mechanical as well as chemical bonding. The rate of diffusion of aluminum into the nickel-chomi- Aum alloy coating is substantially greater that that of the nickel-chromium alloy into the base metal, so that at elevated preheat temperatures of about 1200 to l400 F. some interdiffusion occurs during the application of the aluminum to the metal article.
After the aluminum spray coating has been applied, -the coated object is heated to a temperature within the range of from 1500 to 2100 F. and maintained at that temperature for a period of from a few seconds to five minutes to achieve controlled diffusion and alloying of the aluminum into the nickel-chromium alloy coating and forming therewith an extremely hard corrosionand wear- Vresistant coating. The diffusion time required is depend- 'ent on the diffusion temperature, as well as the preheat temperature of the metallic object during the spray ap- "plication of the aluminum. If, for example, the aluminum is applied to the coated object, pre-heated to a temperature of about l400 F., a substantial interdiffusion is achieved during the application of the aluminum with a lesser amount of subsequent diffusion required. In addition, during the period required to heat the aluminum coated metal article up to the diffusion treatment temperature, more interdiffusion will occur between the aluminum and nickel-chromium alloy, the extent of which is dependent on the rate of heating and time required to attain the vappropriate temperature. The total on combined interdiffusion of the nickel-chromium and aluminum coatings is controlled so as to produce an alloy layer of the desired composition and hardness and which is extremely resistant to vcorrosion and wear. Moreover, the thickness of the interdiffused layer should be at least about 0.0003 inch thick to provide sufficient protection but, preferably, not greater than 0.004 inch thick, because of the brittle nature of the interdiffused alloy. By controlling the thickness of the interdiffused alloy layer to about 0.004 inch or less, the brittle alloy responds in a more ductile manner, thereby greatly increasing its wear and impact Iesistance.
The fact that partial'interdiffusion of the aluminum voccurs, during 'theV application of the aluminum to the nickel-chromium alloy coating forming therewith a substantially' tenacious' bond provides additional processing l,flexibility in that the diffusion step may either immedi- 'ately follow the aluminizing coating or may be deferred to a later time, if desired, without risk of separation or flking ofthe outer aluminum coating.
An enlarged fragmentary view of a base metal having 'thereon an 'interdiffused alloy layer of aluminum, nickel and chromiumrisshown'in FIGURE 2. The diffused alloy layer is designated by the numeral 13 while the undiffused outer layer comprised predominantly of aluminum and oxides thereof is designated 14. The undiifused portion of the underlying nickel-chromium alloy coating 11 is bonded to the base metal 10 by means of chemical bond 12. It will, of course, be appreciated that the principal zones or layers on the surface of the base metal are not as definitive as shown in FIGURE 2, but rather, in actual practice, the layers gradually blend one into the other vwithout a definite line of demarcation. Hardness determinations lobtained with a Rockwell testing apparatus of the interdiffused alloy layer indicate the hardness to range from approximately 48 to 62 Rockwell C. X-ray diffraction analyses made of the composition of this unique corrosionand wear-resistant layer produced varying diffraction patterns, indicating that the alloy lacks chemical homogeneity. These X-ray studies further indicated that the predominant phase in the hard alloy layer is based on the space lattice Al3(Ni,Cr)2. In addition, the coating contains appreciable quantities of a second phase comprised of aluminum oxide in the form A1203 in amounts up to about l0 weight percent. The aluminum oxide as well as lesser quantities of nickel and chromium oxides are formed during the spray application of the coatings and during subsequent diffusions at elevated temperatures 1n air.
One of the specific applications of this invention relates to the corrosion and wear protection of engine valves, particularly the exhaust valves of an internal combustion engine. It is well known that commercial gasolines inherently contain constituents such as sulfur which, on combustion, produce corrosive elements such as sulfur dioxide which have a deleterious effect on the metal objects they contact. In addition, most gasolines also contain small quantities of special additives, such as tetraethyl lead, as an anti-knock agent, halogenated hydrocarbons as scavengers for the lead oxide formed from tetra- -ethyl lead during combustion, and phosphorus-containing compounds to inhibit pre-ignition and spark plug fouling. These additives, although effective to achieve their intended purpose, are highly corrosive and attack the surface of engine valves exposed tothe high temperature exhaust gases with a resultant pitting and flaking of the valve, materially shortening its effective operating life.
By applying a corrosionand wear-resistant surface coating on the heads and/ or faces of the valves in accordance with the preferred practice of this invention, engine valves can be produced which are highly resistant to corrosion and Wear under these severe operating conditions. Most engine valves are of a ferrous or nickel base stainless alloy having, the requisite oxidation resistance suitable for applying the nickel-chromium alloy coating in accordance with the processing sequence heretofore described. Valves in engines which are subjected to only moderate operating severity, such as in most passenger automobiles, normally do not require additional corrosion protection beyond that afforded by the valve material. However, in modern high-compression ratio passenger car engines, iron oxide formation on the head face of the valve promotes pre-ignition, a Very damaging form of combustion. Accordingly, a coating of nickel-chromium alloy over the head portion of the valve exposed to the high temperature exhaust gases is sufficient to prevent formation of the' iron oxide scale. Valves in heavy-duty engine operation, as encountered in airplanes and in trucks, for example, generally require corrosion and Wear protection of the seat face of the valve and head corrosion protection to assure a long and efficient operating life. The seat face of the valve is, of course, that portion of the valve which is in contact with the valve seat, forming therewith a pressure-tight seal. When applying a corrosionand wear-resistant seat facing to a valve, it is preferred to machine the face of the valve after applying the nickelchromium alloy coating and-prior to applying the aluminum coating to assure satisfactory dimensional control. Surface finishing the face of the valve after the application and controlled diffusion of the thin aluminum coating is generally not necessary. A light surface finshing operation to remove high spots is permissible but a deep surface finishing operation is undesirable, due to the possibility of removing all or a portion of the hard nickel chromium aluminum alloy layer.
Engine dynamometer studies under accelerated test conditions designed to evaluate the relative operating life of exhaust valves of the same base material indicated that 'valves having a protective coating on their heads comprised of 80 nickel, 20 chromium alloy to inhibit head corrosion and applied in accordance with the preferred practice of this invention had effective operating lives about four times greater than the same valves in an uncoated condition. Similar accelerated engine tests designed to evaluate the relative effectiveness of a corrosionand wear-resistant coating comprised of interdiifused aluminum and nickel-chromium alloy applied to the seat face of a valve indicated that the coated valve had an operating life prior to failure approximately five times greater than the same valve in an uncoated condition.
A typical processing sequence for applying a corrosionand wear-resistant coating to the base of a valve is comprised of taking the valve that has been machined roughly to size and cleaning the surface to be coated by degreasing and grit blasting. The cleaned valve is next inserted so that its head is surrounded by an induction coil providing localized heating, whereby the surface to be coated is raised to a temperature of approximately 1700 F. within about fifteen seconds and a nickel-chromium alloy sprayed on the face of said valve immediately after its withdrawal from the coil. Immediately after application of the nickelchromium spray coating, the head of the valve is reinserted in the induction coil and heated to a diffusion temperature of approximately 2100 F. for a period of about one minute, and then permitted to cool gradually in air prior to machining. After the coated valve has been machined and degreased, the head is reinserted in an induction coil, whereby it is preheated to approximately 500 F. in a matter of seconds, and then withdrawn from the coil to permit an aluminum sprayy coating to be applied over the nickel-chromium alloy coating. T he coated valve is once again reinserted into the induction coil and heated to a temperature of about 2000 F. for a period of approximately four minutes to provide controlled interdiffusion of the aluminum and nickel-chromium alloy coating forming thereby the corrosion and wear resistant layer having a hardness in the range of about 48 to 58 Rockwell C. The valve is then permitted to cool gradually in air to room temperature, at which time it is ready for use.
Variations to this processing sequence include the application of the nickel-chromium corrosion-resistant alloy to the head as Well as to the seat face of the valve in cases where head corrosion protection is also desired. Moreover, instead of applying a spray coating of aluminum to only the seat face of the valve, it may be desired to also apply a protective coating of aluminum on the head portion of the valve, which may be either uncoated or coated with the nickel-chromium alloy and in which case it is preferred to dip the entire head of the valve in a bath of molten aluminum. The individual treating steps are, of course, adaptable to integration by automation whereby the metallic article or valve to be coated can be automatically processed starting with the uncoated object through to the nished product.
While it will be apparent that the preferred embodiment herein illustrated is well calculated to fulfill the objects above stated, it will be appreciated that the invention is susceptible to modification, variation and change without departing from he proper scope or fair meaning of the subjoined claims.
What is claimed is: 1. A process for applying a coating on at least a portion of a metallic surface, said metallic surface being suiiiciently resistant to corrosion that substantially no oxide will form thereon during the period required to rapidly heat said surface in air to a temperature in the range of about 1300 to about 1800 F., comprising the l.steps of preheating said surface in air to a temperature in the range of about 1300 to about 1800e F., metal spraying at least a portion of the metallurgically clean preheated surface with an alloy containing at least weight percent of the elements nickel and chromium, said nickel content ranging from about 97 to about 70 Weight percent, said chromium content ranging from abou 3 to about 30 weight percent, heating said coated `surface to a temperature in the range of about 1800 to about 2250 F. for a period of time suiiicient to interdiifuse and alloy said coating with said metallic surface thereby tenaciously bonding said coating to said surface, applying a coating comprised predominantly of aluminum over said bonded nickel chromium alloy coating, heating said coated surface to a temperature in the range of about 1500 to about 2100 F. for a period of from a few seconds to about five minutes and forming thereby a hard, interdit-fused alloy layer comprised predominantly of aluminum, nickel and chromium.
2. A process for applying a coating on at least a portion of a metallic surface, said metallic surface being sufficiently resistant to corrosion that substantially no oxide will form thereon during the period required to rapidly heat said surface in air to a temperature in the range of about 1300 to about 1800 F., comprising the steps of preheating said surface in air to a temperature in the range of about 1300 to about 1800 F., metal spraying at least a portion of the metallurgically clean preheated surface with an alloy containing at least 90 weight percent of the elements nickel and chormium, said nickel content rang- Iing from about 97 to about 70* weight percent, said chromium content ranging from about 3 to about 30 weight percent, heating said coated surface to a temperature in the range of about 1800 to about 2250 F. for a period of from about one to about five minutes so as to interdiifuse and alloy said coating with said metallic surface thereby tenaciously bonding said coating to said surface, heating said coated surface to a temperature in the range of about 300 to about 1400" F., superimposing a coating containing at least about 90 weight percent aluminum over said preheated underlying nickel chromium alloy coating, heating said coated surface to a temperature in the range of about 1500 to about 2100 F. for a period sufficient to interdiffuse and alloy said outer aluminum coating with said underlying nickel chromium alloy coating forming thereby an alloy layer of the type A13 (Ni,Cr)2 and to a thickness between about 0.0003 to about 0.004 inch.
References Cited UNITED STATES PATENTS 1,578,254. 3/1926 Bennett.
2,300,400 11/1942 Axline 117-71 2,414,923 1/ 1947 Batcheller 117-50 2,757,445 8/1956 Anger 117-71 X 2,809,127 10/1957 Gibson 117-71 2,917,818 12/1959 Thomson 117-71 X 3,010,480 11/1961 Ragsdale 117-71 X 3,053,689 9/1962 Shoudy et al. 117-71 ALFRED L. LEAVITT, Primary Examiner.
I. R. BATTEN, JR., Assistant Examiner,
Claims (1)
1. A PROCESS FOR APPLYING A COATING ON AT LEAST A PORTION OF A METALLIC SURFACE, SAID METALLIC SURFACE BEING SUFFICIENTLY RESISTANT TO CORROSION THAT SUBSTANTIALLY NO OXIDE WILL FORM THEREON DURING THE PERIOD REQUIRED TO RAPIDLY HEAT SAID SURFACE IN AIR TO A TEMPERATURE IN THE RANGE OF ABOUT 1300 TO ABOUT 1800*F., COMPRISING THE STEPS OF PREHEATING SAID SURFACE IN AIR TO A TEMPERATURE IN THE RANGE OF ABOUT 1300 TO ABOUT 1800*F., METAL SPRAYING AT LEAST A PORTION OF THE METALLURGICALLY CLEAN PREHEATED SURFACE WITH AN ALLOY CONTAINING AT LEAST 90 WEIGHT PERCENT OF THE ELEMENTS NICKEL AND CHROMIUM, SAID NICKEL CONTENT RANGING FROM ABOUT 97 TO ABOUT 70 WEIGHT PERCENT, SAID CHROMIUM CONTENT RANGING FROM ABOUT 3 TO ABOUT 30 WEIGHT PERCENT, HEATING SAID COATED SURFACE TO A TEMPERATURE IN THE RANGE OF ABOUT 1800 TO ABOUT 2250*F. FOR A PERIOD OF TIME SUFFICIENT TO INTERDIFFUSE AND ALLOY SAID COATING WITH SAID METALLIC SURFACE THEREBY TENACIOUSLY BONDING SAID COATING TO SAID SURFACE, APPLYING A COATING COMPRISED PREDOMINANTLY OF ALUMINUM OVER SAID BONDED NICKEL CHROMIUM ALLOY COATING, HEATING SAID COATED SURFACE TO A TEMPERATURE IN THE RANGE OF ABOUT 1500 TO ABOUT 2100*F. FOR A PERIOD OF FROM A FEW SECONDS TO ABOUT FIVE MINUTES AND FORMING THEREBY A HARD, INTERDIFFUSED ALLOY LAYER COMPRISED PREDOMINANTLY OF ALUMINUM, NICKEL AND CHROMIUM.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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GB3566/60A GB949612A (en) | 1959-06-26 | 1960-02-01 | A process for supplying a coating on at least a portion of a metallic surface and a metal article produced in such process |
US343174A US3338733A (en) | 1959-06-26 | 1963-12-30 | Method of coating metallic surfaces with layers of nickel-chromium and aluminum |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US823214A US3165823A (en) | 1959-06-26 | 1959-06-26 | Metallic surface coating and method for making the same |
US343174A US3338733A (en) | 1959-06-26 | 1963-12-30 | Method of coating metallic surfaces with layers of nickel-chromium and aluminum |
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US3338733A true US3338733A (en) | 1967-08-29 |
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US343174A Expired - Lifetime US3338733A (en) | 1959-06-26 | 1963-12-30 | Method of coating metallic surfaces with layers of nickel-chromium and aluminum |
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Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3656919A (en) * | 1965-11-01 | 1972-04-18 | Avco Corp | Composite metal having a nickel alloy base with a diffused coating |
US3887731A (en) * | 1973-04-23 | 1975-06-03 | Chromalloy American Corp | Corrosion resistant coating system for ferrous metal articles having brazed joints |
US3998603A (en) * | 1973-08-29 | 1976-12-21 | General Electric Company | Protective coatings for superalloys |
US4024294A (en) * | 1973-08-29 | 1977-05-17 | General Electric Company | Protective coatings for superalloys |
US4041196A (en) * | 1974-09-18 | 1977-08-09 | Alloy Surfaces Company, Inc. | Diffusion treatment of metal |
US4219592A (en) * | 1977-07-11 | 1980-08-26 | United Technologies Corporation | Two-way surfacing process by fusion welding |
US4601999A (en) * | 1983-11-09 | 1986-07-22 | William B. Retallick | Metal support for a catalyst |
US4743514A (en) * | 1983-06-29 | 1988-05-10 | Allied-Signal Inc. | Oxidation resistant protective coating system for gas turbine components, and process for preparation of coated components |
US4826738A (en) * | 1987-07-07 | 1989-05-02 | United Technologies Corporation | Oxidation and corrosion resistant chromia forming coatings |
US4829655A (en) * | 1987-03-24 | 1989-05-16 | W. R. Grace & Co.-Conn. | Catalyst support and method for making same |
US5691004A (en) * | 1996-07-11 | 1997-11-25 | Ford Global Technologies, Inc. | Method of treating light metal cylinder bore walls to receive thermal sprayed metal coatings |
US20100308491A1 (en) * | 2009-06-05 | 2010-12-09 | Boehler Schmiedetechnik Gmbh & Co Kg | Method for hot shaping a workpiece and agent for reducing the heat emission |
US20150321233A1 (en) * | 2012-07-20 | 2015-11-12 | Nippon Steel & Sumitomo Metal Corporation | Piercing plug |
EP3080321A4 (en) * | 2013-12-10 | 2017-08-09 | Lei Chen | Electrodeposited nickel-chromium alloy |
EP3080338A4 (en) * | 2013-12-10 | 2017-08-09 | Lei Chen | Nickel-chromium-aluminum composite by electrodeposition |
US10233677B2 (en) * | 2013-07-17 | 2019-03-19 | Johnson Controls Gmbh | Locking mechanism with increased safety feature |
US10378118B2 (en) | 2013-12-11 | 2019-08-13 | United Technologies Corporation | Electroformed nickel-chromium alloy |
US10871124B2 (en) * | 2018-08-02 | 2020-12-22 | Ford Global Technologies, Llc | Coated valve seat region of an internal combustion engine |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4163071A (en) * | 1977-07-05 | 1979-07-31 | Union Carbide Corp | Method for forming hard wear-resistant coatings |
US4475991A (en) * | 1983-03-25 | 1984-10-09 | Chugai Denki Kogyo K.K. | Method of diffusion cladding a Fe-containing base material for decorative articles and ornaments with precious metal constituents including Ag |
FR2606037B1 (en) * | 1986-11-04 | 1989-02-03 | Total Petroles | METAL COATING MADE ON A MINERAL SUBSTRATE |
GB2313382A (en) * | 1996-05-23 | 1997-11-26 | Vidal Henri Brevets | Metal coating |
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US3053689A (en) * | 1958-07-09 | 1962-09-11 | Gen Motors Corp | Process of coating austenitic steel with chromium alloy coatings |
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Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3656919A (en) * | 1965-11-01 | 1972-04-18 | Avco Corp | Composite metal having a nickel alloy base with a diffused coating |
US3887731A (en) * | 1973-04-23 | 1975-06-03 | Chromalloy American Corp | Corrosion resistant coating system for ferrous metal articles having brazed joints |
US3998603A (en) * | 1973-08-29 | 1976-12-21 | General Electric Company | Protective coatings for superalloys |
US4024294A (en) * | 1973-08-29 | 1977-05-17 | General Electric Company | Protective coatings for superalloys |
US4041196A (en) * | 1974-09-18 | 1977-08-09 | Alloy Surfaces Company, Inc. | Diffusion treatment of metal |
US4219592A (en) * | 1977-07-11 | 1980-08-26 | United Technologies Corporation | Two-way surfacing process by fusion welding |
US4743514A (en) * | 1983-06-29 | 1988-05-10 | Allied-Signal Inc. | Oxidation resistant protective coating system for gas turbine components, and process for preparation of coated components |
US4601999A (en) * | 1983-11-09 | 1986-07-22 | William B. Retallick | Metal support for a catalyst |
US4829655A (en) * | 1987-03-24 | 1989-05-16 | W. R. Grace & Co.-Conn. | Catalyst support and method for making same |
US4826738A (en) * | 1987-07-07 | 1989-05-02 | United Technologies Corporation | Oxidation and corrosion resistant chromia forming coatings |
US5691004A (en) * | 1996-07-11 | 1997-11-25 | Ford Global Technologies, Inc. | Method of treating light metal cylinder bore walls to receive thermal sprayed metal coatings |
US8685298B2 (en) * | 2009-06-05 | 2014-04-01 | Boehler Schmiedetechnik Gmbh & Co Kg | Method for hot shaping a workpiece and agent for reducing the heat emission |
US20100308491A1 (en) * | 2009-06-05 | 2010-12-09 | Boehler Schmiedetechnik Gmbh & Co Kg | Method for hot shaping a workpiece and agent for reducing the heat emission |
US9440283B2 (en) | 2009-06-05 | 2016-09-13 | Boehler Schmiedetechnik Gmbh & Co. Kg | Method for hot shaping a workpiece and agent for reducing the heat emission |
US20150321233A1 (en) * | 2012-07-20 | 2015-11-12 | Nippon Steel & Sumitomo Metal Corporation | Piercing plug |
US10150147B2 (en) * | 2012-07-20 | 2018-12-11 | Nippon Steel & Sumitomo Metal Corporation | Piercing plug |
US10233677B2 (en) * | 2013-07-17 | 2019-03-19 | Johnson Controls Gmbh | Locking mechanism with increased safety feature |
EP3080321A4 (en) * | 2013-12-10 | 2017-08-09 | Lei Chen | Electrodeposited nickel-chromium alloy |
EP3080338A4 (en) * | 2013-12-10 | 2017-08-09 | Lei Chen | Nickel-chromium-aluminum composite by electrodeposition |
US10669867B2 (en) | 2013-12-10 | 2020-06-02 | Raytheon Technologies Corporation | Electrodeposited nickel-chromium alloy |
US10669851B2 (en) | 2013-12-10 | 2020-06-02 | Raytheon Technologies Corporation | Nickel-chromium-aluminum composite by electrodeposition |
US10378118B2 (en) | 2013-12-11 | 2019-08-13 | United Technologies Corporation | Electroformed nickel-chromium alloy |
US11732372B2 (en) | 2013-12-11 | 2023-08-22 | Raytheon Technologies Corporation | Electroformed nickel-chromium alloy |
US10871124B2 (en) * | 2018-08-02 | 2020-12-22 | Ford Global Technologies, Llc | Coated valve seat region of an internal combustion engine |
Also Published As
Publication number | Publication date |
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GB949612A (en) | 1964-02-12 |
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