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.