US20020098392A1 - Modified boron containing coating for improved wear and pitting resistance - Google Patents
Modified boron containing coating for improved wear and pitting resistance Download PDFInfo
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- US20020098392A1 US20020098392A1 US10/105,536 US10553602A US2002098392A1 US 20020098392 A1 US20020098392 A1 US 20020098392A1 US 10553602 A US10553602 A US 10553602A US 2002098392 A1 US2002098392 A1 US 2002098392A1
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- coating
- boron
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- 238000000576 coating method Methods 0.000 title claims abstract description 116
- 239000011248 coating agent Substances 0.000 title claims abstract description 106
- 150000001638 boron Chemical class 0.000 title description 3
- 229910052810 boron oxide Inorganic materials 0.000 claims abstract description 25
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 22
- 239000000463 material Substances 0.000 claims abstract description 7
- 229910052580 B4C Inorganic materials 0.000 claims description 24
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 21
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 17
- 229910052796 boron Inorganic materials 0.000 claims description 17
- 229910052582 BN Inorganic materials 0.000 claims description 5
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000005137 deposition process Methods 0.000 claims 8
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 229910001882 dioxygen Inorganic materials 0.000 claims 1
- 238000005096 rolling process Methods 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 description 15
- 239000010410 layer Substances 0.000 description 11
- 238000005240 physical vapour deposition Methods 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000005461 lubrication Methods 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000012300 argon atmosphere Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000004626 scanning electron microscopy Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 238000004876 x-ray fluorescence Methods 0.000 description 2
- 238000005452 bending Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Images
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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
- C23C14/5846—Reactive treatment
- C23C14/5853—Oxidation
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/0635—Carbides
-
- 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
- C23C26/00—Coating not provided for in groups C23C2/00 - C23C24/00
-
- 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
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
-
- 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
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
- C23C28/04—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
Definitions
- This invention relates generally to a method of making a metallic article being coated to have enhanced wear resistance and an increased pitting resistance.
- lubricated concentrated rolling contacts can fail from surface or subsurface initiated pitting. Sliding contacts can fail from excessive wear, scuffing or seizure. These failure mechanisms are controlled globally by oil film thickness, hertzian contact stresses, and lubrication at asperity contacts. These factors, in conjunction with other factors, determine the distribution of contact stresses near asperities, friction coefficient, and contact flash temperature. All of these factors will influence pitting and wear failures.
- Meshing of teeth contact surfaces in gears usually operate in the region of mixed-film lubrication where the film thickness to roughness ratio, lambda, is less than three. This results in the load being shared between the fluid and the asperity contact.
- the lubrication behavior in this region is influenced by the overall distributions of lubricant film thickness, pressure, shear stress and flash temperatures within the hertzian contact and the local variation of these quantities around the asperity contacts.
- the present invention is directed to overcoming one or more of the problems as set forth above.
- the invention may be characterized as a modified boron coated metallic component having improved enhanced wear resistance and increased pitting resistance.
- the component comprises a metallic substrate, a first coating (e.g. boron carbide), a second coating (e.g. an mixture of boron carbide and boron oxide) and a third coating(e.g. boron oxide) deposited on the substrate.
- the first coating has a thickness generally no greater than about 3.0 microns.
- the second coating has a thickness no greater than 1 micron.
- the third coating has a thickness generally no greater than about 0.5 microns.
- a coated wear resistant metallic article and method of making the article of this invention comprises a basic article, a first coating material, a second coating, and a third coating.
- the basic article is a metallic material, preferably steel.
- the first coating material is a non-oxide boron containing coating, preferably boron carbide.
- the second coating is a mixture of the non-oxide boron containing coating and boron oxide.
- the third coating material is boron oxide.
- a further aspect of the invention is that the disclosed coatings of the metallic component operate to augment the wear resistance and pitting resistance of the component. This can significantly reduce the possibility of failures of the metallic component.
- FIG. 1 is a side view of a coated metallic article
- FIG. 2 is a cross-sectional view of a coated metallic article in accordance with the present invention.
- FIG. 1 there is shown a side view of a coated metallic piece in accordance with the present invention.
- the illustrated metallic piece 2 includes a main body section 4 , a first end section 6 , and a second end section 8 .
- the various sections are formed or machined from a metallic substrate, 10 , preferably steel.
- the metallic piece is used for a wear component, such as a gear.
- Composition of the first coating 12 is preferably selected from the group consisting of non-oxide boron containing coatings, and in particular, boron carbide or boron nitride.
- the first coating thickness should be fairly uniform as measured by the Ball Crater Test at a plurality of locations on the component. Alternatively, one can demonstrate uniform coating thickness through scanning electron microscopy measurements on a sample of selected cross sections of the coated component, or with X-ray fluorescence.
- the first coating 12 has a thickness desirably no greater than about 3.0 microns and preferably has a thickness of between about 1.0 microns and about 3.0 microns.
- a first coating thickness greater than about 3.0 microns is undesirable because the first coating may disbond from the surface.
- Composition of a second coating 14 consists of a mixture of boron carbide and boron oxide. The composition of this mixture will gradually change from 100% boron carbide to 100% boron oxide.
- the coating thickness of the second coating 14 should be no greater than 1.0 microns, and preferably has a thickness between about 0.5 to 1.0 microns.
- Composition of the third coating 16 consists of boron oxide.
- the coating thickness of the third coating 16 should be no greater than 0.5 microns, and preferably has a thickness between about 0.2-0.5 microns.
- the third coating 16 thickness should be fairly uniform as by the Ball Crater Test at a plurality of locations. Alternatively, one can demonstrate uniform third coating thickness through scanning electron microscopy measurements on a sample of selected cross sections of the fuel injector plungers, or through the use of X-ray fluorescence.
- any one of the vapor deposition techniques such as physical vapor deposition (e.g. sputtering) or chemical vapor deposition can be employed to deposit the first, second, and third coatings on the metallic substrate.
- the first non-oxide boron containing coating is deposited by physical vapor deposition (PVD) process.
- the second and third boron oxide coatings are created by increasing the oxygen partial pressure at the conclusion of the physical vapor deposition (PVD) process.
- the first non-oxide boron containing coating is formed on the surface of the metallic substrate by transferring either boron carbide or boron from a target.
- the first non-oxide boron containing coating is transferred from a target, argon is added to the atmosphere to form a non-reactive atmosphere to prevent the reduction of the boron carbide and to insure the proper composition is deposited on the metallic substrate.
- boron is transferred from a target, methane or propane is added to the atmosphere to react with the borom and form boron carbide on the surface of the metallic substrate.
- the second layer that consists of a mixture of boron carbide and boron oxide.
- the composition of the second layer will gradually be changed from non-oxide boron containing coating to boron oxide until the third layer, which is formed on top of the second layer, will be 100% boron oxide.
- the first, second, and third coatings may be applied by the chemical vapor deposition (CVD) process.
- CVD chemical vapor deposition
- a boron containing gas with methane on the surface of the substrate reacts to form the non-oxide boron containing first coating layer.
- oxygen is added, replacing the methane, to first form a mixture of the non-oxide boron containing coating and oxide.
- the third boron oxide coating 16 may be formed by heating the first non-oxide boron containing coating 12 to above 500 degrees C. for about 1 hour in an oxidizing atmosphere. Similar to the above embodiment, a second coating 14 consisting of a mixture of non-oxide boron containing compound and oxide is formed. Then, upon further heating and oxidation, a continuous third boron oxide coating 16 , 0.2-5 micron thick, is formed.
- a cross-sectional drawing of the metallic piece 2 includes the metallic substrate, 10 , preferably steel, the first coating 12 , second coating 14 , and the third coating 16 .
- a gear is placed into a reactive chamber after properly cleaning the surface. After pulling a vacuum to approximately 10 ⁇ 5 torr a boron carbide coating is deposited on the surface of the gear teeth by a sputtering method. In this method energetic ions are accelerated towards a boron carbide target. The sputtered boron carbide molecules are then directed to and condensed (deposited) on the surface of interest. This process is carried out in a non-reactive argon atmosphere. A typical deposition rate is 0.1 micron per minute.
- the modified boron coating is formed by gradually introducing oxygen into the argon atmosphere after approximate 20 minutes or after a 2.0 micron thick boron carbide coating has been applied to the surface.
- the oxygen introduction will occur over the last 10 minutes of the coating deposition cycle.
- the composition of the coating will then be gradually changed from boron carbide to boron oxide in the last 0.7 micron of coating thickness.
- the final coating deposited using this method will have a microstructure consisting of 2.0 micron boron carbide, a 0.5 micron gradient layer of boron carbide and boron oxide, and a 0.2 micron layer of boron oxide.
- the component is a metallic substrate 2 , a first coating 12 (e.g. boron carbide), a second coating 14 (e.g. a gradient layer of boron carbide and boron oxide) and a third coating 16 (e.g. boron oxide) deposited on the substrate.
- the first coating 12 has a thickness generally no greater than about 3.0 microns.
- the second coating 14 forms a thickness no greater than 1.0 microns.
- the third coating 16 has a thickness generally no greater than about 0.5 microns.
- the basic articles of the invention of the above described metallic component 2 are shaped to a predetermined form by machining from rolled steel, by casting or forging, by consolidating steel powder, or by a combination of forming operations.
- the surface of the article is coated by physical vapor deposition with a hard coating, preferably selected from the carbides or nitrides, preferably boron carbide.
- a basic article of the invention for example a gear, is formed, and the first coating material 12 is applied to the surface of the metallic component 2 .
- the first coating 12 forms a layer not greater than 3.0 microns in thickness.
- This coating process is carried out until the boron oxide coating covers the entire surface with a conformal layer not greater than 0.5 microns in thickness.
- Articles formed according to the above are particularly useful as gears, pins, bushings, bearing races, and similar articles subjected to a combinations of high bending loads, surface wear and contact fatigue. Further, by so providing the unique coating of this invention, the resultant article yields improved service life and provides for higher power densities.
Abstract
The invention consists of a coated metallic component which exhibits improved wear and pitting resistance, and a method for making the invention. A metallic component is coated with a functionally gradient material utilizing both a non-oxide containing coating and boron oxide coating. This invention is useful for rolling and sliding contacts.
Description
- This invention relates generally to a method of making a metallic article being coated to have enhanced wear resistance and an increased pitting resistance.
- It is well known that lubricated concentrated rolling contacts can fail from surface or subsurface initiated pitting. Sliding contacts can fail from excessive wear, scuffing or seizure. These failure mechanisms are controlled globally by oil film thickness, hertzian contact stresses, and lubrication at asperity contacts. These factors, in conjunction with other factors, determine the distribution of contact stresses near asperities, friction coefficient, and contact flash temperature. All of these factors will influence pitting and wear failures.
- Meshing of teeth contact surfaces in gears usually operate in the region of mixed-film lubrication where the film thickness to roughness ratio, lambda, is less than three. This results in the load being shared between the fluid and the asperity contact. The lubrication behavior in this region is influenced by the overall distributions of lubricant film thickness, pressure, shear stress and flash temperatures within the hertzian contact and the local variation of these quantities around the asperity contacts.
- The combination of rolling and sliding can initiate fatigue cracks at the surface that will result in pit formation. A high percentage of carbides or nitrides produced at the surface of a component result in greater high temperature strength, resistance to wear, and increased pitting life. Currently, non-oxide boron containing coatings, e.g. boron carbide and boron nitrides, are being used to enhance wear resistance in rolling, sliding, and mixed mode contact surfaces as set forth in U.S. Pat. No. 5,549,764 “Wear Resistant Coated Steel Article” which issued Aug. 27, 1996 to Gary L. Biltgen and is assigned to Caterpillar Inc.
- However, in actual practice it has become apparent that additional frictional reduction and wear resistance is desirable.
- The present invention is directed to overcoming one or more of the problems as set forth above.
- The invention may be characterized as a modified boron coated metallic component having improved enhanced wear resistance and increased pitting resistance.
- The component comprises a metallic substrate, a first coating (e.g. boron carbide), a second coating (e.g. an mixture of boron carbide and boron oxide) and a third coating(e.g. boron oxide) deposited on the substrate. The first coating has a thickness generally no greater than about 3.0 microns. The second coating has a thickness no greater than 1 micron. The third coating has a thickness generally no greater than about 0.5 microns.
- In one aspect of the invention, a coated wear resistant metallic article and method of making the article of this invention comprises a basic article, a first coating material, a second coating, and a third coating. The basic article is a metallic material, preferably steel. The first coating material is a non-oxide boron containing coating, preferably boron carbide. The second coating is a mixture of the non-oxide boron containing coating and boron oxide. The third coating material is boron oxide.
- A further aspect of the invention is that the disclosed coatings of the metallic component operate to augment the wear resistance and pitting resistance of the component. This can significantly reduce the possibility of failures of the metallic component.
- FIG. 1 is a side view of a coated metallic article;
- FIG. 2 is a cross-sectional view of a coated metallic article in accordance with the present invention.
- The following description is the best mode presently contemplated for carrying out the invention. This description is not to be taken in a limiting sense, but is made merely for the purpose of describing the general principals of the invention. The scope and breadth of the invention should be determined with reference to the claims.
- Turning to FIG. 1, there is shown a side view of a coated metallic piece in accordance with the present invention. As seen in FIG. 1, the illustrated
metallic piece 2 includes amain body section 4, afirst end section 6, and asecond end section 8. The various sections are formed or machined from a metallic substrate, 10, preferably steel. In this application, the metallic piece is used for a wear component, such as a gear. - Composition of the
first coating 12 is preferably selected from the group consisting of non-oxide boron containing coatings, and in particular, boron carbide or boron nitride. The first coating thickness should be fairly uniform as measured by the Ball Crater Test at a plurality of locations on the component. Alternatively, one can demonstrate uniform coating thickness through scanning electron microscopy measurements on a sample of selected cross sections of the coated component, or with X-ray fluorescence. - In the preferred embodiment, as best shown in FIG. 2, the
first coating 12 has a thickness desirably no greater than about 3.0 microns and preferably has a thickness of between about 1.0 microns and about 3.0 microns. A first coating thickness greater than about 3.0 microns is undesirable because the first coating may disbond from the surface. - Composition of a
second coating 14 consists of a mixture of boron carbide and boron oxide. The composition of this mixture will gradually change from 100% boron carbide to 100% boron oxide. The coating thickness of thesecond coating 14 should be no greater than 1.0 microns, and preferably has a thickness between about 0.5 to 1.0 microns. - Composition of the
third coating 16 consists of boron oxide. The coating thickness of thethird coating 16 should be no greater than 0.5 microns, and preferably has a thickness between about 0.2-0.5 microns. - The
third coating 16 thickness should be fairly uniform as by the Ball Crater Test at a plurality of locations. Alternatively, one can demonstrate uniform third coating thickness through scanning electron microscopy measurements on a sample of selected cross sections of the fuel injector plungers, or through the use of X-ray fluorescence. - Although not shown, it is readily understood by those skilled in the art that in addition to coating a metallic piece, it would be equally advantageous to provide a coating to such components as gears, bushings, pins, and bearing races.
- Any one of the vapor deposition techniques, such as physical vapor deposition (e.g. sputtering) or chemical vapor deposition can be employed to deposit the first, second, and third coatings on the metallic substrate. In the preferred embodiment, the first non-oxide boron containing coating is deposited by physical vapor deposition (PVD) process. In the preferred embodiment, the second and third boron oxide coatings are created by increasing the oxygen partial pressure at the conclusion of the physical vapor deposition (PVD) process.
- The first non-oxide boron containing coating is formed on the surface of the metallic substrate by transferring either boron carbide or boron from a target.
- If the first non-oxide boron containing coating is transferred from a target, argon is added to the atmosphere to form a non-reactive atmosphere to prevent the reduction of the boron carbide and to insure the proper composition is deposited on the metallic substrate.
- If boron is transferred from a target, methane or propane is added to the atmosphere to react with the borom and form boron carbide on the surface of the metallic substrate.
- Then, near the end of the reaction, oxygen is gradually added to the argon to form the second layer that consists of a mixture of boron carbide and boron oxide. The composition of the second layer will gradually be changed from non-oxide boron containing coating to boron oxide until the third layer, which is formed on top of the second layer, will be 100% boron oxide.
- In another aspect of the invention, the first, second, and third coatings may be applied by the chemical vapor deposition (CVD) process. In the chemical vapor deposition process, a boron containing gas with methane on the surface of the substrate reacts to form the non-oxide boron containing first coating layer. Like the physical vapor deposition process, near the end of the reaction, oxygen is added, replacing the methane, to first form a mixture of the non-oxide boron containing coating and oxide.
- In yet another embodiment of the invention, the third
boron oxide coating 16 may be formed by heating the first non-oxideboron containing coating 12 to above 500 degrees C. for about 1 hour in an oxidizing atmosphere. Similar to the above embodiment, asecond coating 14 consisting of a mixture of non-oxide boron containing compound and oxide is formed. Then, upon further heating and oxidation, a continuous thirdboron oxide coating 16, 0.2-5 micron thick, is formed. - Turning again to FIG. 2, a cross-sectional drawing of the
metallic piece 2 includes the metallic substrate, 10, preferably steel, thefirst coating 12,second coating 14, and thethird coating 16. - A gear is placed into a reactive chamber after properly cleaning the surface. After pulling a vacuum to approximately 10−5 torr a boron carbide coating is deposited on the surface of the gear teeth by a sputtering method. In this method energetic ions are accelerated towards a boron carbide target. The sputtered boron carbide molecules are then directed to and condensed (deposited) on the surface of interest. This process is carried out in a non-reactive argon atmosphere. A typical deposition rate is 0.1 micron per minute.
- The modified boron coating is formed by gradually introducing oxygen into the argon atmosphere after approximate 20 minutes or after a 2.0 micron thick boron carbide coating has been applied to the surface. The oxygen introduction will occur over the last 10 minutes of the coating deposition cycle. The composition of the coating will then be gradually changed from boron carbide to boron oxide in the last 0.7 micron of coating thickness. The final coating deposited using this method will have a microstructure consisting of 2.0 micron boron carbide, a 0.5 micron gradient layer of boron carbide and boron oxide, and a 0.2 micron layer of boron oxide.
- Industrial Applicability
- The disclosed coatings for metallic components, such as gears and pins, are particularly useful in applications where component pitting and high wear are typically encountered.
- The component is a
metallic substrate 2, a first coating 12 (e.g. boron carbide), a second coating 14 (e.g. a gradient layer of boron carbide and boron oxide) and a third coating 16 (e.g. boron oxide) deposited on the substrate. Thefirst coating 12 has a thickness generally no greater than about 3.0 microns. Thesecond coating 14 forms a thickness no greater than 1.0 microns. Thethird coating 16 has a thickness generally no greater than about 0.5 microns. - The basic articles of the invention of the above described
metallic component 2 are shaped to a predetermined form by machining from rolled steel, by casting or forging, by consolidating steel powder, or by a combination of forming operations. - After shaping the basic article, the surface of the article is coated by physical vapor deposition with a hard coating, preferably selected from the carbides or nitrides, preferably boron carbide.
- In particular, a basic article of the invention, for example a gear, is formed, and the
first coating material 12 is applied to the surface of themetallic component 2. Thefirst coating 12 forms a layer not greater than 3.0 microns in thickness. - Near the end of the formation of the first
coated layer 12; oxygen is added to the reaction and ansecond layer 14 containing a mixture of the first non-oxide boron containing coating and boron oxide is present. Upon further oxidation, athird surface layer 16 is formed comprising boron oxide. - This coating process is carried out until the boron oxide coating covers the entire surface with a conformal layer not greater than 0.5 microns in thickness.
- Articles formed according to the above are particularly useful as gears, pins, bushings, bearing races, and similar articles subjected to a combinations of high bending loads, surface wear and contact fatigue. Further, by so providing the unique coating of this invention, the resultant article yields improved service life and provides for higher power densities.
- Other aspects, objects and advantages of this invention can be obtained from a study of the drawings, disclosure and the appended claims.
Claims (15)
1. A component comprising:
a metallic substrate;
a first coating deposited on said metallic substrate using a deposition process, said first coating having a pre-established thickness, said pre-established thickness being in the range up to 3.0 microns;
a second coating deposited on said first coating using a deposition process, said second coating having a pre-established thickness, said pre-established thickness being in the range of up to 1.0 microns; and
a third coating deposited on said second coating using a deposition process, said third coating having a pre-established thickness, said pre-established thickness being in the range of up to 0.5 microns.
2. The component as in claim 1 , wherein said first coating is selected from the group consisting of a non-oxide boron containing coating.
3. The component as in claim 2 , wherein said first coating is boron carbide.
4. The component as in claim 2 , wherein said first coating is boron nitride.
5. The component as in claim 1 , wherein said third coating is boron oxide.
6. A method for reducing the coefficient of friction at the interface of a metallic substrate movably positioned in contacting relation to a second metallic substrate, said method comprising:
preparing a metallic substrate;
depositing a first coating in a coating chamber on said metallic substrate using a deposition process, said first coating having a pre-established thickness, said pre-established thickness being in the range of up to 3.0 microns;
introducing an oxygen gas into said coating chamber during said deposition process;
forming a second coating on said first coating using said deposition process said second coating being a functionally gradient material, said second coating having a pre-established thickness, said pre-established thickness up to 1.0 microns;
forming a third coating on said second coating using said deposition process said second coating being a functionally gradient material, said third coating having a pre-established thickness, said pre-established thickness up to 0.5 microns.
7. The method as in claim 6 , wherein said first coating is selected from the group consisting of non-oxide containing coatings.
8. The method as in claim 7 , wherein said first coating is boron carbide.
9. The method as in claim 7 , wherein said first coating is boron nitride.
10. The method as in claim 6 , wherein said first coating is third coating is boron oxide.
11. A method for reducing the coefficient of friction at the interface of metallic substrate movably positioned in contacting relation to a second metallic substrate, said method comprising:
preparing a metallic substrate;
depositing a first coating in a coating chamber on said metallic substrate using a deposition process said first coating having a pre-established thickness, said pre-established thickness being in the range of up to 3.0 microns;
heating said first coating to a temperature above about 500 degrees C. in an oxygenated furnace;
reacting for about 1 hour;
forming a second coating; said second coating having a pre-established thickness, said pre-established thickness up to 1.0 microns;
forming a third coating, said third coating having a pre-established thickness, said pre-established thickness up to 0.5 microns.
12. The method of claim 11 wherein said first coating is selected from the group consisting of non-oxide containing coatings.
13. The method of claim 12 wherein said first coating is boron carbide.
14. The method of claim 12 wherein said first coating is boron nitride.
15. The method of claim 12 where said third coating is boron oxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/105,536 US20020098392A1 (en) | 1999-09-27 | 2002-03-25 | Modified boron containing coating for improved wear and pitting resistance |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/405,770 US6432480B1 (en) | 1999-09-27 | 1999-09-27 | Modified boron containing coating for improved wear and pitting resistance |
US10/105,536 US20020098392A1 (en) | 1999-09-27 | 2002-03-25 | Modified boron containing coating for improved wear and pitting resistance |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US09/405,770 Division US6432480B1 (en) | 1999-09-27 | 1999-09-27 | Modified boron containing coating for improved wear and pitting resistance |
Publications (1)
Publication Number | Publication Date |
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US20020098392A1 true US20020098392A1 (en) | 2002-07-25 |
Family
ID=23605156
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US09/405,770 Expired - Fee Related US6432480B1 (en) | 1999-09-27 | 1999-09-27 | Modified boron containing coating for improved wear and pitting resistance |
US10/105,536 Abandoned US20020098392A1 (en) | 1999-09-27 | 2002-03-25 | Modified boron containing coating for improved wear and pitting resistance |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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US09/405,770 Expired - Fee Related US6432480B1 (en) | 1999-09-27 | 1999-09-27 | Modified boron containing coating for improved wear and pitting resistance |
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US (2) | US6432480B1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070143997A1 (en) * | 2003-09-23 | 2007-06-28 | Daimlerchrysler Ag | Crankshaft comprising a combined gear wheel and method for the production and use of said crankshaft |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4364995A (en) * | 1981-02-04 | 1982-12-21 | Minnesota Mining And Manufacturing Company | Metal/metal oxide coatings |
US4599281A (en) * | 1981-12-24 | 1986-07-08 | Schwartzkopf Development Corporation | Wearing part |
US5282985A (en) * | 1993-06-24 | 1994-02-01 | The United States Of America As Represented By The Secretary Of The Air Force | Lubricant coatings |
US5356727A (en) * | 1989-07-21 | 1994-10-18 | Aerospatiale Societe Nationale Industrielle | Carbonaceous material protected against oxidation by boron carbonitride |
US5549764A (en) * | 1995-04-21 | 1996-08-27 | Caterpillar Inc. | Wear resistant coated steel article |
US5976716A (en) * | 1996-04-04 | 1999-11-02 | Kennametal Inc. | Substrate with a superhard coating containing boron and nitrogen and method of making the same |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5323277A (en) * | 1976-08-14 | 1978-03-03 | Konishiroku Photo Ind Co Ltd | Photomasking material and photomask |
-
1999
- 1999-09-27 US US09/405,770 patent/US6432480B1/en not_active Expired - Fee Related
-
2002
- 2002-03-25 US US10/105,536 patent/US20020098392A1/en not_active Abandoned
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4364995A (en) * | 1981-02-04 | 1982-12-21 | Minnesota Mining And Manufacturing Company | Metal/metal oxide coatings |
US4599281A (en) * | 1981-12-24 | 1986-07-08 | Schwartzkopf Development Corporation | Wearing part |
US5356727A (en) * | 1989-07-21 | 1994-10-18 | Aerospatiale Societe Nationale Industrielle | Carbonaceous material protected against oxidation by boron carbonitride |
US5282985A (en) * | 1993-06-24 | 1994-02-01 | The United States Of America As Represented By The Secretary Of The Air Force | Lubricant coatings |
US5549764A (en) * | 1995-04-21 | 1996-08-27 | Caterpillar Inc. | Wear resistant coated steel article |
US5976716A (en) * | 1996-04-04 | 1999-11-02 | Kennametal Inc. | Substrate with a superhard coating containing boron and nitrogen and method of making the same |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070143997A1 (en) * | 2003-09-23 | 2007-06-28 | Daimlerchrysler Ag | Crankshaft comprising a combined gear wheel and method for the production and use of said crankshaft |
Also Published As
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US6432480B1 (en) | 2002-08-13 |
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