WO2001033091A1 - Antifriction bearing for use in a corrosive environment - Google Patents

Antifriction bearing for use in a corrosive environment Download PDF

Info

Publication number
WO2001033091A1
WO2001033091A1 PCT/US2000/029671 US0029671W WO0133091A1 WO 2001033091 A1 WO2001033091 A1 WO 2001033091A1 US 0029671 W US0029671 W US 0029671W WO 0133091 A1 WO0133091 A1 WO 0133091A1
Authority
WO
WIPO (PCT)
Prior art keywords
race
coating
raceway
carbon
combination according
Prior art date
Application number
PCT/US2000/029671
Other languages
French (fr)
Inventor
Michael D. Drory
Gary L. Doll
Original Assignee
The Timken Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Timken Company filed Critical The Timken Company
Priority to AU14404/01A priority Critical patent/AU1440401A/en
Publication of WO2001033091A1 publication Critical patent/WO2001033091A1/en

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/30Parts of ball or roller bearings
    • F16C33/32Balls
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/30Parts of ball or roller bearings
    • F16C33/58Raceways; Race rings
    • F16C33/62Selection of substances
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C19/00Bearings with rolling contact, for exclusively rotary movement
    • F16C19/02Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows
    • F16C19/04Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows for radial load mainly
    • F16C19/06Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows for radial load mainly with a single row or balls
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C2206/00Materials with ceramics, cermets, hard carbon or similar non-metallic hard materials as main constituents
    • F16C2206/02Carbon based material
    • F16C2206/04Diamond like carbon [DLC]

Definitions

  • This invention relates in general to antifriction bearings for use in corrosive environments, and more particularly to an antifriction bearing of that type which has a carbon-based coating on its critical surface areas.
  • Some devices rotate at high velocities within environments that are rendered corrosive by halogen gases. In order to sustain high velocities, these devices must be supported on antifriction bearings. Typical of such devices are the rotors within excimer lasers. Also equipment used in the semiconductor processing industry utilizes bearings which operate in environments rich in halogens.
  • the typical antifriction bearing for accommodating rotation in a corrosive environment has races formed from stainless steel or a ceramic, such as silicon nitride, and rolling elements that are likewise formed from stainless steel or a ceramic.
  • Low and medium steels, from which conventional bearings are formed react too readily with halogens to serve any useful purpose for bearings that are subjected to halogens. Such bearings deteriorate much too rapidly.
  • Even bearings formed from stainless steel do not resist attack by the more reactive halogen gases, particularly fluorine. Indeed, halogen gases have an affinity for carbides, particularly the carbides of iron and chromium, and when exposed to stainless steel, deplete the steel of those carbides at its surface areas.
  • the steel of the bearing degrades along its surfaces, and at the raceways tend to spall with the movement of the rolling elements over those raceways.
  • Halogen gases particularly fluorine, also attack ceramics, so races and balls formed from silicon nitride also suffer deterioration, but not as readily but ceramics are otherwise not as well-suited for bearings as is stainless steel.
  • Antifriction bearings function best when a lubricant film covers their critical surface areas, and in a ball bearing this includes the raceways of the races and the surfaces of the balls. But traditional greases and halogens are not particularly compatible, for the grease breaks down when churned by the balls in the presence of halogens. To be sure, specialized greases exist for use in bearings that operate in corrosive environments, but even these greases deteriorate in the presence of fluorine.
  • the present invention resides in an antifriction bearing that operates in an environment rendered corrosive by a halogen gas or a hydrohalogen acid.
  • the bearing includes races and rolling elements located between the races. Each race is formed from stainless steel which provides a substrate for a carbon- based coating. The halogen reduces the surface friction of the coating.
  • Fig. 1 is sectional view of an antifriction bearing provided with a coating in accordance with the present invention:
  • Fig. 2 is sectional view of the bearing taken along line 2-2 of Fig. 1 ; and Fig. 3 is sectional view of the coating.
  • an antifriction bearing A (Figs. 1 and 2) has the capacity to operate for extended periods in an environment rendered corrosive by a halogen gas or a hydrohalogen acid.
  • the bearing A along its critical surfaces has a carbon-based coating C (Fig. 3) which, while being amphorous, is extremely hard and firmly bonded so that, in contrast to graphite, it resists flaking or scaling.
  • Halogens, particularly fluorine alter the surface energy of the coating such that its coefficient of friction with respect to most other material, particularly those used in bearings, is reduced.
  • the bearing A has low friction surfaces.
  • the bearing A includes (Figs. 1 and 2) an inner race 2, an outer race 4 which surrounds the inner race 2, yet is spaced from it, and rolling elements in the form of balls 6 located in the annular space between the races 2 and 4. Actually, the balls 6 contact the inner race 2 along a raceway 8 on the race 2 and contact the outer race 4 along a raceway 10 on the race 4.
  • the two raceways 8 and 10, which are the critical surfaces for the races 2 and 4 take the form of grooves that are concave in cross section, with the curvature generally conforming to the curvature of the balls 6.
  • the bearing A includes a cage 12 having pockets which receive the balls 6. The cage 12 maintains the proper spacing between the balls 6.
  • the two races 2 and 4 are formed from a substance, such as stainless steel, that is at least somewhat resistant to attack by halogen gases and hydrohalogen acids.
  • 440C steel represents a suitable stainless steel.
  • the stainless steel of the races 2 and 4 is hardened, at least along the raceways 8 and 10, and that may be achieved by through hardening, induction hardening, or case-carburizing.
  • the balls 6 may likewise be formed from stainless steel, such as 440C steel, that is covered with the coating C or from a ceramic, such as silicon nitride.
  • the cage 14 may also be formed from stainless steel that is covered with the coating C, or it may be formed from a substance of lesser strength which better resists attack by the particular halogen.
  • the carbon-based coating C extends over the entire surface areas of each of the races 2 and 4 and certainly over the raceways 8 and 10.
  • the coating C serves to protect the races 2 and 4 from the deleterious effects of the halogen gas or hydrohalogen acid.
  • the halogen reacts with the coating C to form a haloginated surface - one that has a more favorable surface energy in the sense that friction along it is reduced.
  • the coating C itself serves as a lubricant, eliminating the need for grease or at least reducing the amount of grease required and rendering the depletion of grease less than a catastrophic event.
  • the stainless steel of each races 2 and 4 forms a substrate 18 to which the carbon-based coating C is bonded.
  • the coating C may include an amorphous carbon known as diamond like carbon (DLC).
  • DLC diamond like carbon
  • the coating C is actually stratified. It includes (Fig. 3) a metallic base layer 20 that is against the stainless steel substrate 18, a surface layer 22 that is exposed to the halogen gas or hydrohalogen acid, and an intervening layer 24 between the metallic base layer 20 and the surface layer 22.
  • the thickness of coating C ranges between 0.1 ⁇ m (micrometers) and 2.0 ⁇ m and is preferably about l .O ⁇ m.
  • the base layer 20 is about 10% of the thickness of the coating C, the surface layer 22 between about 70% and 80%, and the intervening layer 24 between about 10% and 20%.
  • the base layer 20 consists of a metal that bonds well and easily to the stainless steel substrate 18 and bonds with carbon and hydrocarbons as well. Suitable metals for the layer 20 include chromium, molybdenum, tungsten and titanium. Whatever the metal, it is applied to the stainless steel substrate 18 preferably by physical vapor deposition. To this end, the substrate 18 is thoroughly cleaned, preferably by sputtering. Then the metal desired for the base layer 20 is introduced into a plasma of inert gas and deposited on the substrate 18 by physical vapor deposition, with the substrate 18 being maintained at a relatively low temperature on the order of 300° F or less. The metal which is deposited diffuses into the substrate 18, establishing a firm bond, and builds up on itself to form the base layer 20.
  • the intervening layer 24 contains the same metal as the base layer 20 and in addition contains carbon and hydrocarbons. It too is deposited by vapor deposition - a combination of physical vapor deposition and chemical vapor deposition. Both the metal and a hydrocarbon, such as methane, ethylene, or acetylene, are introduced into an inert gas plasma which impinges on the base layer 20, depositing the metal along with carbon and hydrocarbons. The hydrocarbon which enters the plasma disassociates and some of the carbon and hydrogen recombines so that the hydrocarbon which is deposited on the base layer 20 is not necessarily the same as the basic hydrocarbon that is introduced into the plasma. As the intervening layer 24 grows, the content of metal is decreased and the content of carbon and hydrocarbons is increased. Where the intervening layer 24 blends into the base layer 20, the composition of the intervening layer 24 is primarily metal, whereas the intervening layer 24 blends into the surface layer 22, the intervening layer 24 is primarily carbon and hydrocarbon.
  • the surface layer 22 consists primarily of carbon and hydrocarbon, but it does have carbides within it. It is derived by chemical vapor deposition. To this end an inert gas plasma is directed at the intervening layer 24. A gaseous hydrocarbon such as methane, ethylene, or acetylene is introduced into the plasma along with minute particles of a metal which will readily unite with carbon to form a hard carbide that is somewhat resistant to attack by halogens. Suitable metals for the particles are tungsten, molybdeum and titanium. The size of the particles should be somewhat less than the thickness of the surface layer 22.
  • the carbons and hydrocarbons produce a somewhat elastic matrix in which the hard carbide particles are embedded.
  • the balls 6 are also formed from stainless steel with the same coating C over the stainless steel.
  • the balls 6 may be formed from silicon nitride, even though at least fluorine will attack it, although somewhat slowly.
  • the cage 12 likewise may be formed from stainless steel that is covered with the coating C. However, the cage 12 does not see the stresses to which the races 2 and 4 and the balls 4 are subjected, and may be formed from different materials as long as the material is capable of resisting corrosion in the presence of halogens. Teflon, which is available from E.I. duPont, is one material suitable for the cage 12.
  • the somewhat elastic matrix holds the carbide particles in place over the stainless steel substrate 18.
  • the carbide particles in turn resist wear.
  • the matrix formed from carbon and hydrocarbons does more than hold the particles in place. It further protects the stainless steel, and the carbides as well, from the reactive halogens - which is particularly important insofar as fluorine and hydrofluoric acid are concerned.
  • the hydrocarbon reacts with halogens, chemically or otherwise, to alter the surface energy of the coating C such that the coefficient of friction between the coating C and that which moves over it, usually the balls 6, is reduced. In other words, in the presence of a halogen, the coating C provides a low friction surface.
  • the carbon-based coating C remains intact until it is eventually worn away, and while it does wear away, the bonds within it remain strong, and it does not flake or scale as would graphite. Moreover, the coating C lasts considerably longer than the special greases which are designed to operate in corrosive environments. Indeed, should the bearing A contain such a grease, it will operate satisfactorily when the grease dissipates. In the absence of grease, the bearing A relies on the low coefficient of friction between the balls 6 and the coating C along the raceways 8 and 10 to maintain friction at acceptable levels within the bearing A.
  • the matrix of the surface layer 22 and intervening layer 24 may contain simply amorphous carbon - albeit diamond-like carbon.
  • the coating C may take the form of synthetic diamonds. A synthetic diamond coating C will at low temperature resist corrosion in the presence of halogens, yet will react with the halogens to produce a low friction surface.
  • the coating C may be applied to races and rolling elements of bearings other than ball bearings, tapered roller bearings, cylindrical roller bearings and spherical roller bearings to name several.

Abstract

An antifriction bearing (A) that operates in an environment rendered corrosive by a halogen gas or a hydrohalogen acid has races (2 and 4) that are formed from stainless steel and rolling elements (6) that roll along opposed raceways (8 and 10) on the races (2 and 4). The stainless steel of the races (2 and 4) constitutes a substrate (18) over which a coating (C) extends, and that coating contains amorphous carbon in the form of diamond-like carbon (DLC) which is hard and firmly bonded, so that it does not flake, and also carbides to better resist wear. The coating (C) may also contain hydrocarbons. Indeed, the amorphous carbon and hydrocarbons form a matrix in which the carbides are embedded.

Description

Antifriction Bearing For Use In A Corrosive Environment
Technical Field
This invention relates in general to antifriction bearings for use in corrosive environments, and more particularly to an antifriction bearing of that type which has a carbon-based coating on its critical surface areas.
Some devices rotate at high velocities within environments that are rendered corrosive by halogen gases. In order to sustain high velocities, these devices must be supported on antifriction bearings. Typical of such devices are the rotors within excimer lasers. Also equipment used in the semiconductor processing industry utilizes bearings which operate in environments rich in halogens.
The typical antifriction bearing for accommodating rotation in a corrosive environment has races formed from stainless steel or a ceramic, such as silicon nitride, and rolling elements that are likewise formed from stainless steel or a ceramic. Low and medium steels, from which conventional bearings are formed, react too readily with halogens to serve any useful purpose for bearings that are subjected to halogens. Such bearings deteriorate much too rapidly. Even bearings formed from stainless steel do not resist attack by the more reactive halogen gases, particularly fluorine. Indeed, halogen gases have an affinity for carbides, particularly the carbides of iron and chromium, and when exposed to stainless steel, deplete the steel of those carbides at its surface areas. The steel of the bearing degrades along its surfaces, and at the raceways tend to spall with the movement of the rolling elements over those raceways. Halogen gases, particularly fluorine, also attack ceramics, so races and balls formed from silicon nitride also suffer deterioration, but not as readily but ceramics are otherwise not as well-suited for bearings as is stainless steel.
Antifriction bearings function best when a lubricant film covers their critical surface areas, and in a ball bearing this includes the raceways of the races and the surfaces of the balls. But traditional greases and halogens are not particularly compatible, for the grease breaks down when churned by the balls in the presence of halogens. To be sure, specialized greases exist for use in bearings that operate in corrosive environments, but even these greases deteriorate in the presence of fluorine.
Most devices having rotors that operate in the presence of halogens have enclosures which isolate their rotors and confine the halogens. Access to a rotor and to the bearings which support it is difficult and requires disassembly of nearby components. Bearing replacement consumes considerable time and requires skilled technicians. As a consequence it is quite costly. Even applying additional grease to the bearings is costly. Background Art
The present invention resides in an antifriction bearing that operates in an environment rendered corrosive by a halogen gas or a hydrohalogen acid. The bearing includes races and rolling elements located between the races. Each race is formed from stainless steel which provides a substrate for a carbon- based coating. The halogen reduces the surface friction of the coating. Brief Description of Drawings
Fig. 1 is sectional view of an antifriction bearing provided with a coating in accordance with the present invention:
Fig. 2 is sectional view of the bearing taken along line 2-2 of Fig. 1 ; and Fig. 3 is sectional view of the coating.
Best Mode for Carrying Out the Invention
Referring to the drawings, an antifriction bearing A (Figs. 1 and 2) has the capacity to operate for extended periods in an environment rendered corrosive by a halogen gas or a hydrohalogen acid. The bearing A along its critical surfaces has a carbon-based coating C (Fig. 3) which, while being amphorous, is extremely hard and firmly bonded so that, in contrast to graphite, it resists flaking or scaling. Halogens, particularly fluorine, alter the surface energy of the coating such that its coefficient of friction with respect to most other material, particularly those used in bearings, is reduced. In short, the bearing A has low friction surfaces.
The bearing A includes (Figs. 1 and 2) an inner race 2, an outer race 4 which surrounds the inner race 2, yet is spaced from it, and rolling elements in the form of balls 6 located in the annular space between the races 2 and 4. Actually, the balls 6 contact the inner race 2 along a raceway 8 on the race 2 and contact the outer race 4 along a raceway 10 on the race 4. The two raceways 8 and 10, which are the critical surfaces for the races 2 and 4, take the form of grooves that are concave in cross section, with the curvature generally conforming to the curvature of the balls 6. In addition, the bearing A includes a cage 12 having pockets which receive the balls 6. The cage 12 maintains the proper spacing between the balls 6.
The two races 2 and 4 are formed from a substance, such as stainless steel, that is at least somewhat resistant to attack by halogen gases and hydrohalogen acids. 440C steel represents a suitable stainless steel. The stainless steel of the races 2 and 4 is hardened, at least along the raceways 8 and 10, and that may be achieved by through hardening, induction hardening, or case-carburizing. The balls 6 may likewise be formed from stainless steel, such as 440C steel, that is covered with the coating C or from a ceramic, such as silicon nitride. The cage 14 may also be formed from stainless steel that is covered with the coating C, or it may be formed from a substance of lesser strength which better resists attack by the particular halogen.
Several of the halogen gases and hydrohalogen acids will attack stainless steel, reacting primarily with carbides of chromium and iron in the steel, particularly at the grain boundaries This produces voids in the steel, so the steel tends to degrade and loose integrity. Actually the degredation is not too significant as to most surface areas on the races 2 and 4, but if it occurs at the raceways 8 and 10, it will adversely affect the operation of the bearing A. After all, the balls 6 roll along the races 2 and 4 at their respective raceways 8 and 10, producing cyclic stresses. If the steel along either raceways 8 or 10 were to degrade, it would spall and transform the otherwise smooth raceways 8 or 10 into a rough surface.
Preferably the carbon-based coating C extends over the entire surface areas of each of the races 2 and 4 and certainly over the raceways 8 and 10. The coating C serves to protect the races 2 and 4 from the deleterious effects of the halogen gas or hydrohalogen acid. Apart from that, the halogen reacts with the coating C to form a haloginated surface - one that has a more favorable surface energy in the sense that friction along it is reduced. Indeed, the coating C itself serves as a lubricant, eliminating the need for grease or at least reducing the amount of grease required and rendering the depletion of grease less than a catastrophic event.
The stainless steel of each races 2 and 4 forms a substrate 18 to which the carbon-based coating C is bonded. The coating C may include an amorphous carbon known as diamond like carbon (DLC). In this form the coating C is actually stratified. It includes (Fig. 3) a metallic base layer 20 that is against the stainless steel substrate 18, a surface layer 22 that is exposed to the halogen gas or hydrohalogen acid, and an intervening layer 24 between the metallic base layer 20 and the surface layer 22. The thickness of coating C ranges between 0.1 μm (micrometers) and 2.0μm and is preferably about l .Oμm. While well-defined boundaries or interfaces do not exist between the layers 20, 22 and 24, inasmuch as adjacent layers blend, the base layer 20 is about 10% of the thickness of the coating C, the surface layer 22 between about 70% and 80%, and the intervening layer 24 between about 10% and 20%.
The base layer 20 consists of a metal that bonds well and easily to the stainless steel substrate 18 and bonds with carbon and hydrocarbons as well. Suitable metals for the layer 20 include chromium, molybdenum, tungsten and titanium. Whatever the metal, it is applied to the stainless steel substrate 18 preferably by physical vapor deposition. To this end, the substrate 18 is thoroughly cleaned, preferably by sputtering. Then the metal desired for the base layer 20 is introduced into a plasma of inert gas and deposited on the substrate 18 by physical vapor deposition, with the substrate 18 being maintained at a relatively low temperature on the order of 300° F or less. The metal which is deposited diffuses into the substrate 18, establishing a firm bond, and builds up on itself to form the base layer 20.
The intervening layer 24 contains the same metal as the base layer 20 and in addition contains carbon and hydrocarbons. It too is deposited by vapor deposition - a combination of physical vapor deposition and chemical vapor deposition. Both the metal and a hydrocarbon, such as methane, ethylene, or acetylene, are introduced into an inert gas plasma which impinges on the base layer 20, depositing the metal along with carbon and hydrocarbons. The hydrocarbon which enters the plasma disassociates and some of the carbon and hydrogen recombines so that the hydrocarbon which is deposited on the base layer 20 is not necessarily the same as the basic hydrocarbon that is introduced into the plasma. As the intervening layer 24 grows, the content of metal is decreased and the content of carbon and hydrocarbons is increased. Where the intervening layer 24 blends into the base layer 20, the composition of the intervening layer 24 is primarily metal, whereas the intervening layer 24 blends into the surface layer 22, the intervening layer 24 is primarily carbon and hydrocarbon.
The surface layer 22 consists primarily of carbon and hydrocarbon, but it does have carbides within it. It is derived by chemical vapor deposition. To this end an inert gas plasma is directed at the intervening layer 24. A gaseous hydrocarbon such as methane, ethylene, or acetylene is introduced into the plasma along with minute particles of a metal which will readily unite with carbon to form a hard carbide that is somewhat resistant to attack by halogens. Suitable metals for the particles are tungsten, molybdeum and titanium. The size of the particles should be somewhat less than the thickness of the surface layer 22.
The plasma transforms the metal hydrocarbon into carbon and different hydrocarbons and some of the carbon unites with the metal of the particles to form hard carbide particles. The carbons and hydrocarbons produce a somewhat elastic matrix in which the hard carbide particles are embedded. Preferably the balls 6 are also formed from stainless steel with the same coating C over the stainless steel. The low friction surfaces formed by the coatings C on the raceways 8 and 10 and the coatings C on, the balls 6, when in the presence of a halogen such as fluorine, produces a well-lubricated bearing A, even in the absence of traditional forms of lubrication. On the other hand, the balls 6 may be formed from silicon nitride, even though at least fluorine will attack it, although somewhat slowly. The cage 12 likewise may be formed from stainless steel that is covered with the coating C. However, the cage 12 does not see the stresses to which the races 2 and 4 and the balls 4 are subjected, and may be formed from different materials as long as the material is capable of resisting corrosion in the presence of halogens. Teflon, which is available from E.I. duPont, is one material suitable for the cage 12.
In the operation of the bearing A, the somewhat elastic matrix holds the carbide particles in place over the stainless steel substrate 18. The carbide particles in turn resist wear. But the matrix formed from carbon and hydrocarbons does more than hold the particles in place. It further protects the stainless steel, and the carbides as well, from the reactive halogens - which is particularly important insofar as fluorine and hydrofluoric acid are concerned. Moreover, the hydrocarbon reacts with halogens, chemically or otherwise, to alter the surface energy of the coating C such that the coefficient of friction between the coating C and that which moves over it, usually the balls 6, is reduced. In other words, in the presence of a halogen, the coating C provides a low friction surface.
The carbon-based coating C remains intact until it is eventually worn away, and while it does wear away, the bonds within it remain strong, and it does not flake or scale as would graphite. Moreover, the coating C lasts considerably longer than the special greases which are designed to operate in corrosive environments. Indeed, should the bearing A contain such a grease, it will operate satisfactorily when the grease dissipates. In the absence of grease, the bearing A relies on the low coefficient of friction between the balls 6 and the coating C along the raceways 8 and 10 to maintain friction at acceptable levels within the bearing A.
In lieu of having a carbon-hydrocarbon constituency, the matrix of the surface layer 22 and intervening layer 24 may contain simply amorphous carbon - albeit diamond-like carbon. In lieu of diamond-like carbon together with hydrocarbons and metal carbides, the coating C may take the form of synthetic diamonds. A synthetic diamond coating C will at low temperature resist corrosion in the presence of halogens, yet will react with the halogens to produce a low friction surface.
The coating C may be applied to races and rolling elements of bearings other than ball bearings, tapered roller bearings, cylindrical roller bearings and spherical roller bearings to name several.

Claims

Claims:
1. In combination with an environment rendered corrosive by the presence of a halogen gas or a hydrohalogen acid, an antifriction bearing comprising: a first race having a raceway; a second race having a raceway presented opposite, yet spaced from, the raceway of the first race; and rolling elements located between raceways of the two races, such that when the first race rotates relative to the second race the rolling elements will roll along the raceways, at least one of the races having a coating along its raceway, with the coating comprising a substantial proportion of amorphous carbon.
2. The combination according to Claim 1 wherein the coating contains diamond-like carbon.
3. The combination according to Claim 1 wherein the races are formed from stainless steel.
4. The combination according to Claim 3 wherein the coating is on each race at its raceway, and the stainless steel forms a substrate on the race.
5. The combination according to Claim 4 wherein the coating comprises a metal base layer bonded to the substrate of the race on which the coating is located, a carbon-based surface layer exposed to and in contact with the rolling elements, and an intervening layer which contains both metal and carbon, but proportionally less metal than the base layer and less carbon than the surface layer.
6. The combination according to Claim 5 wherein the surface layer contains amorphous carbon and hydrocarbons and also carbides.
7. The combination according to Claim 6 wherein the base layer is selected from a group consisting of chromium, tungsten, molybdenum, and titanium.
8. The combination according to Claim -1 wherein the atmosphere is rich in fluorine.
9. The combination according to Claim 1 wherein the coating extends along each race at its raceway.
10. The combination according to Claim 9 wherein each rolling element includes a stainless steel substrate and a carbon-based coating over that substrate.
1 1. In combination with an environment that is rich in fluorine, an antifriction bearing comprising: a first race providing a substrate formed from stainless steel and having a raceway and a carbon-based coating over the substrate at the raceway; a second race providing a substrate formed from stainless steel and having a raceway and a carbon-based coating over the substrate at that raceway, the raceway on the second race being presented toward the raceway on the first race, and rolling elements located between the races at their raceways and bearing against the coatings at the raceways, such that when one race rotates relative to the other race the rolling elements roll along the coatings at the raceways.
12. The combination according to Claim 11 wherein the coating along its exposed surface includes an amorphous carbon and carbides embedded in the amorphous carbon.
13. The combination according to Claim 12 wherein the coating also includes hydrocarbons.
PCT/US2000/029671 1999-10-29 2000-10-26 Antifriction bearing for use in a corrosive environment WO2001033091A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU14404/01A AU1440401A (en) 1999-10-29 2000-10-26 Antifriction bearing for use in a corrosive environment

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16262899P 1999-10-29 1999-10-29
US60/162,628 1999-10-29

Publications (1)

Publication Number Publication Date
WO2001033091A1 true WO2001033091A1 (en) 2001-05-10

Family

ID=22586453

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2000/029671 WO2001033091A1 (en) 1999-10-29 2000-10-26 Antifriction bearing for use in a corrosive environment

Country Status (2)

Country Link
AU (1) AU1440401A (en)
WO (1) WO2001033091A1 (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1262674A2 (en) * 2001-05-29 2002-12-04 NSK Ltd., Rolling sliding member and rolling apparatus
DE10145405A1 (en) * 2001-09-14 2003-04-03 Fraunhofer Ges Forschung Rolling bearing used in cylinder rollers comprises an inner and an outer running ring each having a running path arranged opposite each other and arranged between rolling bodies
NL1019860C2 (en) * 2002-01-30 2003-08-05 Skf Ab Roller bearing with a ceramic rolling element and steel inner or outer ring.
WO2003085276A3 (en) * 2002-04-02 2004-04-08 Timken Co Full complement antifriction bearing
DE10259003A1 (en) * 2002-12-16 2004-06-24 Myonic Gmbh Slide bearing, in particular to be used in dental tool, comprising parts permanently coated with lubricant of suitable kind
WO2004090361A3 (en) * 2003-04-03 2004-11-18 Timken Co Corrosion tolerant rolling element bearing
DE102006057484A1 (en) * 2006-12-06 2008-06-19 Schaeffler Kg Rolling bearings with a surface coating
WO2008106330A1 (en) * 2007-02-28 2008-09-04 The Timken Company Bi-directional tapered roller bearing assembly with improved wear resistance
US20100034495A1 (en) * 2005-08-01 2010-02-11 Aktiebolaget Skf Bearing and method of producing the same
DE102009060924A1 (en) * 2009-12-18 2011-06-22 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V., 80686 A structure containing a solid lubricant (solid lubricant structure), in particular a solid lubricant structure formed for a vacuum tribological application, and a production method thereof
WO2011120866A1 (en) 2010-04-01 2011-10-06 Aktiebolaget Skf Bearing ring of a plain or rolling bearing
DE102010030648A1 (en) * 2010-06-29 2011-12-29 Bayerische Motoren Werke Aktiengesellschaft Taper roller bearing for use in e.g. wheel bearing of passenger car, has inner ring comprising ring outer side functioning bearing surface, where portion of surface of rolling element is provided with low-friction coating
DE102011017776A1 (en) 2011-04-29 2012-10-31 Schaeffler Technologies AG & Co. KG Bearing with corrosion-protected bearing part
CN110630641A (en) * 2018-06-21 2019-12-31 斯凯孚公司 Rolling bearing assembly

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06193637A (en) * 1992-12-25 1994-07-15 Ntn Corp Rolling bearing
JPH06341445A (en) * 1991-10-14 1994-12-13 Shojiro Miyake Rolling bearing
JPH0994911A (en) * 1995-09-29 1997-04-08 Ntn Corp Rigid carbon film molded product
WO1999014512A1 (en) * 1997-09-16 1999-03-25 Skf Engineering & Research Centre B.V. Coated rolling element bearing
JP2000049140A (en) * 1998-07-27 2000-02-18 Speedfam-Ipec Co Ltd Semiconductor manufacturing equipment
JP2000136828A (en) * 1998-11-04 2000-05-16 Koyo Seiko Co Ltd Rolling bearing

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06341445A (en) * 1991-10-14 1994-12-13 Shojiro Miyake Rolling bearing
JPH06193637A (en) * 1992-12-25 1994-07-15 Ntn Corp Rolling bearing
JPH0994911A (en) * 1995-09-29 1997-04-08 Ntn Corp Rigid carbon film molded product
WO1999014512A1 (en) * 1997-09-16 1999-03-25 Skf Engineering & Research Centre B.V. Coated rolling element bearing
JP2000049140A (en) * 1998-07-27 2000-02-18 Speedfam-Ipec Co Ltd Semiconductor manufacturing equipment
JP2000136828A (en) * 1998-11-04 2000-05-16 Koyo Seiko Co Ltd Rolling bearing

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 018, no. 548 (M - 1689) 19 October 1994 (1994-10-19) *
PATENT ABSTRACTS OF JAPAN vol. 1995, no. 03 28 April 1995 (1995-04-28) *
PATENT ABSTRACTS OF JAPAN vol. 1997, no. 08 29 August 1997 (1997-08-29) *
PATENT ABSTRACTS OF JAPAN vol. 2000, no. 05 14 September 2000 (2000-09-14) *
PATENT ABSTRACTS OF JAPAN vol. 2000, no. 08 6 October 2000 (2000-10-06) *

Cited By (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6994474B2 (en) 2001-05-29 2006-02-07 Nsk Ltd. Rolling sliding member and rolling apparatus
EP1873412A1 (en) * 2001-05-29 2008-01-02 NSK Ltd. Rolling sliding member and rolling apparatus
CN100398861C (en) * 2001-05-29 2008-07-02 日本精工株式会社 Rolling sliding member and rolling apparatus
EP1870609A1 (en) 2001-05-29 2007-12-26 NSK Ltd. Rolling sliding member and rolling apparatus
US7172343B2 (en) 2001-05-29 2007-02-06 Nsk Ltd. Rolling sliding member and rolling apparatus
EP1262674A3 (en) * 2001-05-29 2006-10-04 NSK Ltd. Rolling sliding member and rolling apparatus
EP1262674A2 (en) * 2001-05-29 2002-12-04 NSK Ltd., Rolling sliding member and rolling apparatus
DE10145405A1 (en) * 2001-09-14 2003-04-03 Fraunhofer Ges Forschung Rolling bearing used in cylinder rollers comprises an inner and an outer running ring each having a running path arranged opposite each other and arranged between rolling bodies
WO2003064874A1 (en) * 2002-01-30 2003-08-07 Ab Skf Rolling bearing having ceramic rolling element and steel inner or outer ring
NL1019860C2 (en) * 2002-01-30 2003-08-05 Skf Ab Roller bearing with a ceramic rolling element and steel inner or outer ring.
US6764219B2 (en) 2002-04-02 2004-07-20 The Timken Company Full complement antifriction bearing
WO2003085276A3 (en) * 2002-04-02 2004-04-08 Timken Co Full complement antifriction bearing
DE10259003A1 (en) * 2002-12-16 2004-06-24 Myonic Gmbh Slide bearing, in particular to be used in dental tool, comprising parts permanently coated with lubricant of suitable kind
WO2004090361A3 (en) * 2003-04-03 2004-11-18 Timken Co Corrosion tolerant rolling element bearing
US8383239B2 (en) * 2005-08-01 2013-02-26 Aktiebolaget Skf Bearing and method of producing the same
US20100034495A1 (en) * 2005-08-01 2010-02-11 Aktiebolaget Skf Bearing and method of producing the same
DE102006057484A1 (en) * 2006-12-06 2008-06-19 Schaeffler Kg Rolling bearings with a surface coating
WO2008068130A3 (en) * 2006-12-06 2009-01-22 Schaeffler Kg Rolling bearing with a surface coating
DE102006057484B4 (en) * 2006-12-06 2010-05-12 Schaeffler Kg Rolling bearings with a surface coating
US8496382B2 (en) 2007-02-28 2013-07-30 The Timken Company Bi-directional tapered roller bearing assembly with improved wear resistance
WO2008106330A1 (en) * 2007-02-28 2008-09-04 The Timken Company Bi-directional tapered roller bearing assembly with improved wear resistance
EP2607725A3 (en) * 2007-02-28 2013-12-25 The Timken Company Roller bearing assembly with improved wear resistance
DE102009060924A1 (en) * 2009-12-18 2011-06-22 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V., 80686 A structure containing a solid lubricant (solid lubricant structure), in particular a solid lubricant structure formed for a vacuum tribological application, and a production method thereof
DE102009060924B4 (en) * 2009-12-18 2017-01-26 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Production Method for a Solid Lubricant Structure A solid lubricant structure produced by the production method, and uses
WO2011120866A1 (en) 2010-04-01 2011-10-06 Aktiebolaget Skf Bearing ring of a plain or rolling bearing
DE102010013630A1 (en) * 2010-04-01 2011-10-06 Aktiebolaget Skf Bearing ring of a sliding or roller bearing
DE102010030648A1 (en) * 2010-06-29 2011-12-29 Bayerische Motoren Werke Aktiengesellschaft Taper roller bearing for use in e.g. wheel bearing of passenger car, has inner ring comprising ring outer side functioning bearing surface, where portion of surface of rolling element is provided with low-friction coating
DE102011017776A1 (en) 2011-04-29 2012-10-31 Schaeffler Technologies AG & Co. KG Bearing with corrosion-protected bearing part
WO2012146485A1 (en) 2011-04-29 2012-11-01 Schaeffler Technologies AG & Co. KG Bearing comprising a corrosion-resistant bearing part
US8961030B2 (en) 2011-04-29 2015-02-24 Schaeffler Technologies AG & Co. KG Bearing comprising a corrosion-resistant bearing part
CN110630641A (en) * 2018-06-21 2019-12-31 斯凯孚公司 Rolling bearing assembly

Also Published As

Publication number Publication date
AU1440401A (en) 2001-05-14

Similar Documents

Publication Publication Date Title
US6340245B1 (en) Coated rolling element bearing
US6764219B2 (en) Full complement antifriction bearing
US6517249B1 (en) Bearing with amorphous boron carbide coating
WO2001033091A1 (en) Antifriction bearing for use in a corrosive environment
JPH09133138A (en) Bearing device
EP1078171B1 (en) Coated rolling element bearing
WO2011122662A1 (en) Anti-friction bearing
WO2013042765A1 (en) Hard film, hard film formed body, and rolling bearing
US5163757A (en) Metal oxide lubrication for ceramic bearing system
US20200408261A1 (en) Rolling bearing and method of manufacturing the same
JP5993680B2 (en) Rolling bearing and manufacturing method thereof
US6234679B1 (en) Rolling bearing with coated element
JPH06341445A (en) Rolling bearing
EP3845769B1 (en) Double-row self-aligning roller bearing and main shaft support device for wind generation equipped with same
JP2020118292A (en) Rolling bearing and wind power generation spindle support device
WO2018164139A1 (en) Rolling bearing and method for producing same
JP2007155022A (en) Rolling device
Hintermann et al. Wear-resistant coatings for bearing applications
WO2000037813A1 (en) Ball bearing
JP2012067900A (en) Rolling bearing
JP2007127263A (en) Rolling member and rolling device
JPS62258224A (en) Bearing
JPH1047359A (en) Rolling bearing
JP5620860B2 (en) Rolling bearing
JP2008151264A (en) Cage for roller bearing

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: JP