The present disclosure relates generally to turbocharger housings with a conversion coating, and methods of making the conversion coating.
Turbochargers for diesel engines control the amount of turbo boost by controlling the flow of exhaust gas onto the turbine blades. Such control is accomplished by an internal actuator that opens and closes a set of vanes that are collectively held by a unison ring. A linear actuator pushes on a slot in the unison ring, which is constrained on its inside diameter by a machined feature on the turbocharger center housing. The constraint causes the linear motion to be converted to rotational motion.
A turbocharger includes a center housing having a bearing surface configured to contact an inner surface of a unison ring. A conversion coating is impregnated onto the bearing surface of the center housing.
Features and advantages of examples of the present disclosure will become apparent by reference to the following detailed description and drawings, in which like reference numerals correspond to similar, though perhaps not identical, components. For the sake of brevity, reference numerals or features having a previously described function may or may not be described in connection with other drawings in which they appear.
Failed turbochargers often result from the vanes sticking in undesirable positions. It is believed that the present inventors have discovered at least one of the heretofore unknown causes of the sticking vanes. As shown in the example below, the inventors have found that sticking vanes are the result of corrosion and wear of the turbocharger housing at the point where a loaded unison ring contacts the turbocharger housing. In order to reduce or eliminate the corrosion and wear that leads to sticking vanes, and thus extend the service life of the turbocharger, the inventors are passivating at least the portion of the turbocharger housing that contacts the unison ring. The added coating advantageously reduces the friction between the unison ring and a bearing surface of the turbocharger housing which contacts the unison ring.
In
The turbocharger center housing 12 is formed of nodular iron (ductile iron) or stainless steel. Nodular iron is suitable for the turbocharger center housing 12, at least in part because nodular iron may be exposed to operating conditions (e.g., extreme temperatures) that are not suitable for other iron materials, such as, for example, grey cast iron. Furthermore, nodular iron may be treated by heat treatments or chemical conversion processes, such as those described herein, to improve performance.
The turbocharger center housing 12 disclosed herein includes a conversion coating 18 (shown as speckles) impregnated into at least the bearing surface S. In some instances, the entire center housing 12, including the bearing surface S (also referred to herein as the hub) and the groove G, may have the conversion coating 18 impregnated therein. The surface of the housing 12 into/on which the conversion coating 18 is formed may be a finished machined surface (i.e., additional machining is not needed), or an unfinished machined surface (i.e., additional machining may be desirable).
It is believed that the conversion coating 18 will reduce or eliminate corrosion and wear of the turbocharger center housing 12, and thus reduce or eliminate the undesirable sticking of the vanes. Still further, it is believed that the conversion coating 18 increases the turbocharger's ability to withstand thermal cycles having temperatures ranging from about 700° C. to about 780° C. Other wear resistant coatings, such as chemical or physical vapor deposited diamond-like carbon or transition metal nitrides, or thermal sprayed coatings, are deleteriously affected by such conditions due, at least in part, to coefficient of thermal expansion mismatches and/or adhesion issues. Since the conversion coating 18 disclosed herein is integral with the metal of the turbocharger center housing 12, it is further believed that it is not susceptible to delamination.
A non-limiting example of such a conversion coating 18 is formed via ferritic nitrocarburizing. The ferritic nitrocarburizing process is accomplished at temperatures below the service temperature of the turbocharger 10 (i.e., the temperature conditions to which the turbocharger 10 is exposed when in use in a vehicle), which ranges from about 700° C. to about 800° C. The lower temperatures advantageously keep the turbocharger center housing 12 from warping during processing.
While a ferritic nitrocarburizing process is described further hereinbelow, it is believed that other methods of nitriding may also be used to form the conversion coating 18. Examples of such other processes include gas nitrocarburizing or plasma nitrocarburizing.
Any of the nitrocarburizing processes disclosed herein may include a cleaning and pre-heating cycle (which takes place at about 400° C.). This cycle substantially ensures that at least the bearing surface S (or the entire surface of the center housing 12) is clean and dry. When the ferritic nitrocarburizing process is used, the pre-treatment process is also believed to reduce thermal shock and permit more efficient recovery of the nitrocarburizing bath temperature.
Since the present inventors found that the bearing surface S is the portion of the center housing 12 that deleteriously affects the vanes, it is desirable to form the conversion coating 18 at this portion of the housing. As such, a mask (examples of which are discussed hereinbelow) may be used to selectively form the coating 18 on the bearing surface S, while the remainder of the housing 12 is uncoated. However, it is believed that the conversion coating 18 does not deleteriously affect the remainder of the housing 12, and as such, the coating 18 may be formed on the entire housing 12 surface (including the groove G).
When forming the coating 18 via plasma nitrocarburizing, a masking process may be utilized to selectively form the conversion coating 18 on particular surfaces of the center housing 12. Using plasma nitrocarburizing, it is to be understood that the coating 18 forms where the ion current flows to the surfaces. As such, masking may be used to control the voltage and current flow to the surfaces, thus controlling the coating 18 location. Such techniques may be particularly suitable when it is desirable to form the conversion coating 18 on the bearing surface S alone. In one instance, masking may be accomplished by physically encasing the surfaces of the center housing 12 where plasma nitrocarburizing treatment is undesirable. For example, all surfaces of the center housing 12 except for the bearing surface S may be covered by the mask (not shown), which may be shaped like a box that surrounds the desirable surfaces. The exposed bearing surface S and the mask will be exposed to the plasma nitrocarburizing process, but the surfaces underlying or surrounded by the mask will remain untreated. A non-limiting example of such a physical mask is formed of a conductor material, such as, for example, low carbon steel (e.g., 1020) or stainless steel (e.g., 303 and 304). Generally, aluminum and galvanized steel are not suitable masking materials. In another instance, masking may be accomplished by insulating one or more of the surfaces where plasma nitrocarburizing treatment is undesirable. When the surface(s) are insulated, the ion current is not able to flow to such surfaces, and thus such surface(s) remain untreated. Non-limiting examples of the insulating mask include a refractory (ceramic) cloth or wool (e.g., KAOWOOL® available from Thermal Ceramics Inc., Augusta, Ga.) or ceramic plugs. Insulating materials/masks may be incorporated into one or more holes of the surfaces that are to remain untreated.
In an example in which the conversion coating 18 is applied to the entire housing 12 surface, the housing 12 is exposed to a gas nitrocarburizing process. Using gas nitrocarburizing, it is to be understood that the coating 18 forms where the gas reacts with the exposed surfaces.
In another example in which the conversion coating 18 is applied to the entire housing 12 surface, the housing 12 is immersed into a nitrocarburizing salt bath such that each surface is exposed to the contents of the bath for a predetermined time. It is to be understood that the time of exposure to the nitrocarburizing salt bath depends, at least in part, on the desirable depth for the conversion coating 18 into the housing 12.
The liquid salt bath obtains its source of nitrogen and carbon through sodium and potassium salts containing cyanates (CNO—) and carbonates. The non-cyanide salts are formulated to be fluidic at the processing temperature (580° C.), and to generate nitrogen and carbon activity within the bath, thus producing a desired epsilon iron nitride. It is to be understood that the nitrogen and carbon activity may be controlled by monitoring and regulating the cyanate concentration. As the center housing 12 is immersed into the liquid bath, the following catalytic reaction occurs at the surface, whereby the cyanate breaks down to release nitrogen and carbon. Both elements diffuse into the housing 12 surface causing a change in the element concentration at the surface and within the subjacent zone.
A non-limiting example of the reactions that takes place are:
8CNO—=2CO3=+4CN—+CO2+4N+C 1)
4N+12Fe=4Fe3N 2)
C+3Fe=Fe3C 3)
After the predetermined time for the nitrocarburizing salt bath has expired, the center housing 12 is quenched into an oxidizing salt bath at a lower temperature, for example, 400° C., for a predetermined time. In a non-limiting example, the exposure to the oxidizing bath ranges from about 5 minutes to about 20 minutes. It is believed that the intermediate quenching using the oxidizing bath reduces the cooling rate of the housing 12, thereby mitigating thermally induced distortion.
After the oxidizing quench, the center housing 12 is cooled to room temperature and is rinsed. In some instances, it may be desirable to perform post treatment processes, such as, for example, mechanical polishing or other machining processes.
The result of the above ferritic nitrocarburizing method is a compound layer of iron and nitrogen/carbon at the treated surface of the center housing 12. This compound layer includes predominantly epsilon iron nitride, a phase generally identified as Fe3N. A relatively small volume of gamma prime iron nitride (Fe4N) may also be present at the interface of the base metal and compound layer. Subjacent to the compound layer, diffused nitrogen of lower concentration (less than 0.20% just beneath the compound layer) forms a solid solution with the base metal iron. This is generally referred to as the diffusion zone. It is to be understood that the thickness of this zone depends, at least in part, on the time the housing 12 is in the salt bath and the activity of the salt bath. In some instances, the thickness of the diffusion zone is about 15 microns or less.
The conversion coating 18 may also include microporosity, which varies in depth depending, at least in part, on the materials used and the process parameters/conditions.
To further illustrate the present disclosure, an example is given herein. It is to be understood that this example is provided for illustrative purposes and is not to be construed as limiting the scope of the present disclosure.
An analysis of components from failed turbochargers illustrated to the inventors that the vane sticking problem is caused, at least in part, by corrosion and wear of the turbocharger housing at the point where the loaded unison ring contacts it.
The samples evaluated were housings and rings from vehicles with sticking vanes. The housing hub and unison ring inner diameter were in contact with each other in the vehicle. Some scratching between the parts was noted, and the ring did not rotate freely around the hub except in an arc limited by the vane length (approx. 2 inches). The area of greatest wear is generally where the exhaust gas enters the housing and pushes the unison ring against the hub. The rings samples were previously ion nitrided to prevent wear between the ring and a separate pin, however, the hardened ring was scratching against the hub.
The housings and rings were analyzed using scanning electron microscopy.
It is to be understood that the term “connect/connected” or the like is broadly defined herein to encompass a variety of divergent connection arrangements and assembly techniques. These arrangements and techniques include, but are not limited to (1) the direct connection between one component and another component with no intervening components therebetween; and (2) the connection of one component and another component with one or more components therebetween, provided that the one component being “connected to” the other component is somehow operatively connected to the other component (notwithstanding the presence of one or more additional components therebetween).
While several examples have been described in detail, it will be apparent to those skilled in the art that the disclosed examples may be modified. Therefore, the foregoing description is to be considered non-limiting.
This application is a divisional of U.S. patent application Ser. No. 12/326,339, filed on Dec. 2, 2008, now U.S. Pat. No. 8,197,199, issued Jun. 12, 2012, which itself claims the benefit of U.S. Provisional Application Ser. No. 61/059,983, filed Jun. 9, 2008, each of which applications is incorporated herein by reference in its entirety.
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Entry |
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Easterday, J., “Liquid Ferritic Nitrocarburizing”, Nitromet Division of Joleme Corproation, Technology Update, date unknown, pp. 1-10. |
Number | Date | Country | |
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20120227867 A1 | Sep 2012 | US |
Number | Date | Country | |
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61059983 | Jun 2008 | US |
Number | Date | Country | |
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Parent | 12326339 | Dec 2008 | US |
Child | 13481809 | US |